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83-540: Mount Weld mine is a rare earth mine in Western Australia , located about 30 km (20 mi) south of Laverton and 120 km (75 mi) east of Leonora . It is one of the largest rare earth deposits in the world. It is owned by Lynas Corporation . Mining began at the Mount Weld site in 2011. Rare earths are contained in secondary phosphates and aluminophosphates , presumably derived from weathering of

166-549: A fissile material . The principal sources of rare-earth elements are the minerals bastnäsite ( RCO 3 F , where R is a mixture of rare-earth elements), monazite ( XPO 4 , where X is a mixture of rare-earth elements and sometimes thorium), and loparite ( (Ce,Na,Ca)(Ti,Nb)O 3 ), 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

249-595: A CO 2 -rich primary magma, by fractional crystallization of an alkaline primary magma, or by separation of a CO 2 -rich immiscible liquid from. These liquids are most commonly forming in association with very deep Precambrian cratons , like the ones found in Africa and the Canadian Shield. Ferrocarbonatites are the most common type of carbonatite to be enriched in REE, and are often emplaced as late-stage, brecciated pipes at

332-491: A byproduct. The rare earth element neodymium is found in monazite, making it a rare mineral. Moreover, monazite contains many other rare metals such as cerium , lanthanum , praseodymium , and samarium, making it a critical source of renewable energy. Recycled magnets can also be derived from these minerals due to the metals they contain. Monazite sand and deposits for mining are found in India, Brazil, and Australia. Loparite

415-532: A component of magnets in hybrid car motors." The global demand for rare-earth elements (REEs) is expected to increase more than fivefold by 2030. The REE geochemical classification is usually done on the basis of their atomic weight . One of the most common classifications divides REE into 3 groups: light rare earths (LREE - from 57 La to 60 Nd), intermediate (MREE - from 62 Sm to 67 Ho) and heavy (HREE - from 68 Er to 71 Lu). REE usually appear as trivalent ions, except for Ce and Eu which can take

498-657: A few percent of yttrium). Uranium ores from Ontario have occasionally yielded yttrium as a byproduct. Well-known minerals containing cerium, and other LREE, include bastnäsite , monazite , allanite , loparite , ancylite , parisite , lanthanite , chevkinite, cerite , stillwellite , britholite, fluocerite , and cerianite. Monazite (marine sands from Brazil , India , or Australia ; rock from South Africa ), bastnäsite (from Mountain Pass rare earth mine , or several localities in China), and loparite ( Kola Peninsula , Russia ) have been

581-544: A maximum number of 25 was estimated. The use of X-ray spectra (obtained by X-ray crystallography ) by Henry Gwyn Jeffreys Moseley made it possible to assign atomic numbers to the elements. Moseley found that the exact number of lanthanides had to be 15, but that element 61 had not yet been discovered. (This is promethium, a radioactive element whose most stable isotope has a half-life of just 18 years.) Using these facts about atomic numbers from X-ray crystallography, Moseley also showed that hafnium (element 72) would not be

664-432: A melt phase if one is present. REE are chemically very similar and have always been difficult to separate, but the gradual decrease in ionic radius from light REE (LREE) to heavy REE (HREE), called the lanthanide contraction , can produce a broad separation between light and heavy REE. The larger ionic radii of LREE make them generally more incompatible than HREE in rock-forming minerals, and will partition more strongly into

747-404: A melt phase, while HREE may prefer to remain in the crystalline residue, particularly if it contains HREE-compatible minerals like garnet . The result is that all magma formed from partial melting will always have greater concentrations of LREE than HREE, and individual minerals may be dominated by either HREE or LREE, depending on which range of ionic radii best fits the crystal lattice. Among

830-503: A mine in the village of Ytterby in Sweden ; four of the rare-earth elements bear names derived from this single location. A table listing the 17 rare-earth elements, their atomic number and symbol, the etymology of their names, and their main uses (see also Applications of lanthanides ) is provided here. Some of the rare-earth elements are named after the scientists who discovered them, or elucidated their elemental properties, and some after

913-414: A quarry in the village of Ytterby , Sweden and termed "rare" because it had never yet been seen. Arrhenius's "ytterbite" reached Johan Gadolin , a Royal Academy of Turku professor, and his analysis yielded an unknown oxide ("earth" in the geological parlance of the day ), which he called yttria . Anders Gustav Ekeberg isolated beryllium from the gadolinite but failed to recognize other elements in

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996-472: A radioactive tracer. Kyawthuite is a rare earth mineral due to its unique formation process. Unlike other minerals, it is created from a pegmatite deposit within an igneous rock. Its deep red-brown colour and high density come from the crystal assemblages within it. Its occurrence is very limited and the necessary pressure for formation is uncommon, making it quite scarce. The mineral contains lead , thallium , and oxygen that have undergone oxidation and

1079-451: A rare-earth element. Moseley was killed in World War I in 1915, years before hafnium was discovered. Hence, the claim of Georges Urbain that he had discovered element 72 was untrue. Hafnium is an element that lies in the periodic table immediately below zirconium , and hafnium and zirconium have very similar chemical and physical properties. During the 1940s, Frank Spedding and others in

1162-404: A separate group of rare-earth elements (the terbium group), or europium was included in the cerium group, and gadolinium and terbium were included in the yttrium group. In the latter case, the f-block elements are split into half: the first half (La–Eu) form the cerium group, and the second half (Gd–Yb) together with group 3 (Sc, Y, Lu) form the yttrium group. The reason for this division arose from

1245-420: A similar effect. In sedimentary rocks, rare-earth elements in clastic sediments are a representation of provenance. The rare-earth element concentrations are not typically affected by sea and river waters, as rare-earth elements are insoluble and thus have very low concentrations in these fluids. As a result, when sediment is transported, rare-earth element concentrations are unaffected by the fluid and instead

1328-423: A temperature of 400 °C (752 °F). These elements and their compounds have no biological function other than in several specialized enzymes, such as in lanthanide-dependent methanol dehydrogenases in bacteria. The water-soluble compounds are mildly to moderately toxic, but the insoluble ones are not. All isotopes of promethium are radioactive, and it does not occur naturally in the earth's crust, except for

1411-515: A trace amount generated by spontaneous fission of uranium-238 . They are often found in minerals with thorium , and less commonly uranium . Though rare-earth elements are technically relatively plentiful in the entire Earth's crust ( cerium being the 25th-most-abundant element at 68 parts per million, more abundant than copper ), in practice this is spread thin across trace impurities, so to obtain rare earths at usable purity requires processing enormous amounts of raw ore at great expense, thus

1494-457: A valence of 3 and form sesquioxides (cerium forms CeO 2 ). Five different crystal structures are known, depending on the element and the temperature. The X-phase and the H-phase are only stable above 2000 K. At lower temperatures, there are the hexagonal A-phase, the monoclinic B-phase, and the cubic C-phase, which is the stable form at room temperature for most of the elements. The C-phase

1577-562: Is a mineral that contains three rare elements: titanium , niobium , and tantalum . This is why it is often mined, as it is considered a rare-earth mineral. The deposits for loparite can be found in Russia and Paraguay, although it is also present in other countries such as Canada, Norway, Greenland, and Brazil. However, Russia remains the primary source for mining this mineral. The significance of loparite lies in its unique properties, which make it useful for conductivity, aircraft assembly, and as

1660-461: Is called the bixbyite structure, as it occurs in a mineral of that name ( (Mn,Fe) 2 O 3 ). As seen in the chart, rare-earth elements are found on Earth at similar concentrations to many common transition metals. The most abundant rare-earth element is cerium , which is actually the 25th most abundant element in Earth's crust , having 68 parts per million (about as common as copper). The exception

1743-599: Is high, weathering forms a thick argillized regolith, this process is called supergene enrichment and produces laterite deposits; heavy rare-earth elements are incorporated into the residual clay by absorption. This kind of deposit is only mined for REE in Southern China, where the majority of global heavy rare-earth element production occurs. REE-laterites do form elsewhere, including over the carbonatite at Mount Weld in Australia. REE may also be extracted from placer deposits if

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1826-493: Is owned by ASX-listed Lynas Corporation , which raised A$ 450 million equity from J. P. Morgan in 2009 to fund the development of a mine and also a processing plant in Kuantan , Malaysia . Once operational, the Mount Weld mine is expected to be the largest source of rare-earth elements outside of China. Rare-earth element The rare-earth elements ( REE ), also called the rare-earth metals or rare earths , and sometimes

1909-445: Is possible to observe the serial trend of the REE by reporting their normalized concentrations against the atomic number. The trends that are observed in "spider" diagrams are typically referred to as "patterns", which may be diagnostic of petrological processes that have affected the material of interest. According to the general shape of the patterns or thanks to the presence (or absence) of so-called "anomalies", information regarding

1992-458: Is primarily mined for its many purposes. Magnets made of bastnasite are used to create speakers, microphones, communication devices, and many other modern gadgets. This mineral is rare because it contains a large number of rare elements. This mineral can be classified as semi-soluble salt due to its limited solubility in water and capacity to form ionic bonds. Bastnäsite deposits are found in China and

2075-443: Is synthetically produced in nuclear reactors. Due to their chemical similarity, the concentrations of rare earths in rocks are only slowly changed by geochemical processes, making their proportions useful for geochronology and dating fossils. Rare-earth elements occur in nature in combination with phosphate ( monazite ), carbonate - fluoride ( bastnäsite ), and oxygen anions. In their oxides, most rare-earth elements only have

2158-517: Is the highly unstable and radioactive promethium "rare earth" is quite scarce. The longest-lived isotope of promethium has a half-life of 17.7 years, so the element exists in nature in only negligible amounts (approximately 572 g in the entire Earth's crust). Promethium is one of the two elements that do not have stable (non-radioactive) isotopes and are followed by (i.e. with higher atomic number) stable elements (the other being technetium ). The rare-earth elements are often found together. During

2241-448: Is the reason it is mined. This clay-like dirt also makes a stable basis for construction since it solidifies into rock when exposed to air. However, the low fertility of this soil makes it unsuitable for agricultural use. Monazite is a waxy mineral that is formed through the crystallization of igneous rocks and the metamorphism of clastic sedimentary rocks. This mineral is typically mined in placer deposits, with gold commonly found as

2324-563: The Oddo–Harkins rule : even-numbered REE at abundances of about 5% each, and odd-numbered REE at abundances of about 1% each. Similar compositions are found in xenotime or gadolinite. Well-known minerals containing yttrium, and other HREE, include gadolinite, xenotime, samarskite , euxenite , fergusonite , yttrotantalite, yttrotungstite, yttrofluorite (a variety of fluorite ), thalenite, and yttrialite . Small amounts occur in zircon , which derives its typical yellow fluorescence from some of

2407-521: The Proterozoic Mount Weld carbonatite . The primary commercial interest at the site is targeted towards oxides as well as further niobium and tantalum deposits within the intrusive pipe of the Mount Weld carbonatite, which is approximately three kilometers (1.9 mi) in diameter. The main deposits are hosted within the soil and regolith horizon that blankets the entire carbonatite and form shallow lenses within 60 m (200 ft) of

2490-477: The lanthanides or lanthanoids (although scandium and yttrium , which do not belong to this series, are usually included as rare earths), are a set of 17 nearly indistinguishable lustrous silvery-white soft heavy metals . Compounds containing rare earths have diverse applications in electrical and electronic components, lasers, glass, magnetic materials, and industrial processes. Scandium and yttrium are considered rare-earth elements because they tend to occur in

2573-400: The mineral processing of elemental deposits. Various methods, such as leaching and hydrothermal processes, can be employed to extract minerals. Both primary and secondary deposits yield elements and minerals for mining purposes. There are only four rare-earth minerals that are found in deposits that go through certain processes and require mining. Bastnäsite is a carbonate mineral, that

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2656-486: The upper mantle (200 to 600 km depth). This melt becomes enriched in incompatible elements, like the rare-earth elements, by leaching them out of the crystalline residue. The resultant magma rises as a diapir , or diatreme , along pre-existing fractures, and can be emplaced deep in the crust , or erupted at the surface. Typical REE enriched deposits types forming in rift settings are carbonatites, and A- and M-Type granitoids. Near subduction zones, partial melting of

2739-428: The "heavy" group from 6.965 (ytterbium) to 9.32 (thulium), as well as including yttrium at 4.47. Europium has a density of 5.24. Rare-earth elements, except scandium , are heavier than iron and thus are produced by supernova nucleosynthesis or by the s-process in asymptotic giant branch stars. In nature, spontaneous fission of uranium-238 produces trace amounts of radioactive promethium , but most promethium

2822-568: The 4 f orbital which acts against the electrons of the 6 s and 5 d orbitals. The lanthanide contraction has a direct effect on the geochemistry of the lanthanides, which show a different behaviour depending on the systems and processes in which they are involved. The effect of the lanthanide contraction can be observed in the REE behaviour both in a CHARAC-type geochemical system (CHArge-and-RAdius-Controlled ) where elements with similar charge and radius should show coherent geochemical behaviour, and in non-CHARAC systems, such as aqueous solutions, where

2905-498: The LREE. This has economic consequences: large ore bodies of LREE are known around the world and are being exploited. Ore bodies for HREE are more rare, smaller, and less concentrated. Most of the current supply of HREE originates in the "ion-absorption clay" ores of Southern China. Some versions provide concentrates containing about 65% yttrium oxide, with the HREE being present in ratios reflecting

2988-463: The USA. Laterite is considered to be a soil type which holds a significant amount of aluminium and iron. This soil type can form into clay, which holds many minerals within it. The weathering of rocks under leaching and oxidation conditions results in the formation of this mineral soil, which simulates clay. The minerals within this soil are goethite , lepidocrocite , and hematite . In recognition of

3071-515: The United States (during the Manhattan Project ) developed chemical ion-exchange procedures for separating and purifying rare-earth elements. This method was first applied to the actinides for separating plutonium-239 and neptunium from uranium , thorium , actinium , and the other actinides in the materials produced in nuclear reactors . Plutonium-239 was very desirable because it is

3154-449: The accompanying HREE. The zirconium mineral eudialyte , such as is found in southern Greenland , 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 is not as abundant as the similarly recovered monazite (which typically contains

3237-496: The anhydrous rare-earth phosphates, it is the tetragonal mineral xenotime that incorporates yttrium and the HREE, whereas the monoclinic monazite phase incorporates cerium and the LREE preferentially. The smaller size of the HREE allows greater solid solubility in the rock-forming minerals that make up Earth's mantle, and thus yttrium and the HREE show less enrichment in Earth's crust relative to chondritic abundance than does cerium and

3320-402: The case of primary deposits, the minerals and metals are derived from a specific area, where the elements come together to form the deposit. This location is also where the mineral is produced. Derived elements move to a different location within secondary deposits where they undergo metamorphic or sedimentary processes, resulting in the formation of minerals. Mining extractions can benefit from

3403-812: The core of igneous complexes; they consist of fine-grained calcite and hematite, sometimes with significant concentrations of ankerite and minor concentrations of siderite. Large carbonatite deposits enriched in rare-earth elements include Mount Weld in Australia, Thor Lake in Canada, Zandkopsdrift in South Africa, and Mountain Pass in the USA. Peralkaline granites (A-Type granitoids) have very high concentrations of alkaline elements and very low concentrations of phosphorus; they are deposited at moderate depths in extensional zones, often as igneous ring complexes, or as pipes, massive bodies, and lenses. These fluids have very low viscosities and high element mobility, which allows for

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3486-408: The crude yttria 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. Due to the difficulty in separating

3569-735: The crystallization of large grains, despite a relatively short crystallization time upon emplacement; their large grain size is why these deposits are commonly referred to as pegmatites. Economically viable pegmatites are divided into Lithium-Cesium-Tantalum (LCT) and Niobium-Yttrium-Fluorine (NYF) types; NYF types are enriched in rare-earth minerals. Examples of rare-earth pegmatite deposits include Strange Lake in Canada and Khaladean-Buregtey in Mongolia. Nepheline syenite (M-Type granitoids) deposits are 90% feldspar and feldspathoid minerals. They are deposited in small, circular massifs and contain high concentrations of rare-earth-bearing accessory minerals . For

3652-413: The difference in solubility of rare-earth double sulfates with sodium and potassium. The sodium double sulfates of the cerium group are poorly soluble, those of the terbium group slightly, and those of the yttrium group are very soluble. Sometimes, the yttrium group was further split into the erbium group (dysprosium, holmium, erbium, and thulium) and the ytterbium group (ytterbium and lutetium), but today

3735-409: The electron structure is also an important parameter to consider as the lanthanide contraction affects the ionic potential . A direct consequence is that, during the formation of coordination bonds, the REE behaviour gradually changes along the series. Furthermore, the lanthanide contraction causes the ionic radius of Ho (0.901 Å) to be almost identical to that of Y (0.9 Å), justifying the inclusion of

3818-637: The element contained within it is mandatory. If an element can be classified as a rare-earth element, it is more likely to be classified as a rare earth mineral. This information can be valuable in various settings, such as geological surveys and mineral resource assessments. A rare earth element is categorized into sixteen metallic elements. There are over 160 rare earth minerals and only four of these minerals are mined. Most rare earth minerals occur in primary and secondary deposits. Primary deposits contain hydrothermal and igneous processes while secondary deposits are sedimentary and weathering processes. In

3901-651: The element showing the anomaly and the predictable one based on the average of the normalized concentrations of the two elements in the previous and next position in the series, according to the equation: where [ REE i ] n {\displaystyle [{\text{REE}}_{i}]_{n}} is the normalized concentration of the element whose anomaly has to be calculated, [ REE i − 1 ] n {\displaystyle [{\text{REE}}_{i-1}]_{n}} and [ REE i + 1 ] n {\displaystyle [{\text{REE}}_{i+1}]_{n}}

3984-417: The existence of an unknown element. The fractional crystallization of the oxides then yielded europium in 1901. In 1839 the third source for rare earths became available. This is a mineral similar to gadolinite called uranotantalum (now called " samarskite ") an oxide of a mixture of elements such as yttrium, ytterbium, iron, uranium, thorium, calcium, niobium, and tantalum. This mineral from Miass in

4067-511: The following observations apply: anomalies in europium are dominated by the crystallization of feldspars . Hornblende , controls the enrichment of MREE compared to LREE and HREE. Depletion of LREE relative to HREE may be due to the crystallization of olivine , orthopyroxene , and clinopyroxene . On the other hand, the depletion of HREE relative to LREE may be due to the presence of garnet , as garnet preferentially incorporates HREE into its crystal structure. The presence of zircon may also cause

4150-433: The form of Ce and Eu depending on the redox conditions of the system. Consequentially, REE are characterized by a substantial identity in their chemical reactivity, which results in a serial behaviour during geochemical processes rather than being characteristic of a single element of the series. Sc, Y, and Lu can be electronically distinguished from the other rare earths because they do not have f valence electrons, whereas

4233-566: The fractionation of trace elements (including rare-earth elements) into the liquid phase (the melt/magma) into the solid phase (the mineral). If an element preferentially remains in the solid phase it is termed 'compatible', and if it preferentially partitions into the melt phase it is described as 'incompatible'. Each element has a different partition coefficient, and therefore fractionates into solid and liquid phases distinctly. These concepts are also applicable to metamorphic and sedimentary petrology. In igneous rocks, particularly in felsic melts,

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4316-405: The geographical locations where discovered. A mnemonic for the names of the sixth-row elements in order is "Lately college parties never produce sexy European girls that drink heavily even though you look". Rare earths were mainly discovered as components of minerals. Ytterbium was found in the "ytterbite" (renamed to gadolinite in 1800) discovered by Lieutenant Carl Axel Arrhenius in 1787 at

4399-448: The heavy rare-earth elements (HREE), and those that fall in between are typically referred to as the middle rare-earth elements (MREE). Commonly, rare-earth elements with atomic numbers 57 to 61 (lanthanum to promethium) are classified as light and those with atomic numbers 62 and greater are classified as heavy rare-earth elements. Increasing atomic numbers between light and heavy rare-earth elements and decreasing atomic radii throughout

4482-470: The latter among the REE. The application of rare-earth elements to geology is important to understanding the petrological processes of igneous , sedimentary and metamorphic rock formation. In geochemistry , rare-earth elements can be used to infer the petrological mechanisms that have affected a rock due to the subtle atomic size differences between the elements, which causes preferential fractionation of some rare earths relative to others depending on

4565-418: The logarithm to the base 10 of the value. Commonly, the rare-earth elements are normalized to chondritic meteorites , as these are believed to be the closest representation of unfractionated Solar System material. However, other normalizing standards can be applied depending on the purpose of the study. Normalization to a standard reference value, especially of a material believed to be unfractionated, allows

4648-472: The main grouping is between the cerium and the yttrium groups. Today, the rare-earth elements are classified as light or heavy rare-earth elements, rather than in cerium and yttrium groups. The classification of rare-earth elements is inconsistent between authors. The most common distinction between rare-earth elements is made by atomic numbers ; those with low atomic numbers are referred to as light rare-earth elements (LREE), those with high atomic numbers are

4731-522: The metals (and determining the separation is complete), the total number of false discoveries was dozens, with some putting the total number of discoveries at over a hundred. 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 physical process of optical flame spectroscopy and found several new spectral lines in didymia. Also in 1879, Paul Émile Lecoq de Boisbaudran isolated

4814-639: The most part, these deposits are small but important examples include Illimaussaq-Kvanefeld in Greenland, and Lovozera in Russia. Rare-earth elements can also be enriched in deposits by secondary alteration either by interactions with hydrothermal fluids or meteoric water or by erosion and transport of resistate REE-bearing minerals. Argillization of primary minerals enriches insoluble elements by leaching out silica and other soluble elements, recrystallizing feldspar into clay minerals such kaolinite, halloysite, and montmorillonite. In tropical regions where precipitation

4897-415: The name "rare" earths. Because of their geochemical properties, rare-earth elements are typically dispersed and not often found concentrated in rare-earth minerals . Consequently, economically exploitable ore deposits are sparse. The first rare-earth mineral discovered (1787) was gadolinite , a black mineral composed of cerium, yttrium, iron, silicon, and other elements. This mineral was extracted from

4980-560: The new element samarium 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 samarskite. They named the element gadolinium after Johan Gadolin , and its oxide was named " gadolinia ". Further spectroscopic analysis between 1886 and 1901 of samaria, yttria, and samarskite by William Crookes , Lecoq de Boisbaudran and Eugène-Anatole Demarçay yielded several new spectral lines that indicated

5063-424: The normalized concentration, [ REE i ] sam {\displaystyle {[{\text{REE}}_{i}]_{\text{sam}}}} the analytical concentration of the element measured in the sample, and [ REE i ] ref {\displaystyle {[{\text{REE}}_{i}]_{\text{ref}}}} the concentration of the same element in the reference material. It

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5146-427: The normalized concentrations of the respectively previous and next elements along the series. The rare-earth elements patterns observed in igneous rocks are primarily a function of the chemistry of the source where the rock came from, as well as the fractionation history the rock has undergone. Fractionation is in turn a function of the partition coefficients of each element. Partition coefficients are responsible for

5229-432: The observed abundances to be compared to the initial abundances of the element. Normalization also removes the pronounced 'zig-zag' pattern caused by the differences in abundance between even and odd atomic numbers . Normalization is carried out by dividing the analytical concentrations of each element of the series by the concentration of the same element in a given standard, according to the equation: where n indicates

5312-516: The ore. After this discovery in 1794, a mineral from Bastnäs near Riddarhyttan , Sweden, which was believed to be an iron – tungsten mineral, was re-examined by Jöns 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 . It took another 30 years for researchers to determine that other elements were contained in

5395-414: The others do, but the chemical behaviour is almost the same. A distinguishing factor in the geochemical behaviour of the REE is linked to the so-called " lanthanide contraction " which represents a higher-than-expected decrease in the atomic/ionic radius of the elements along the series. This is determined by the variation of the shielding effect towards the nuclear charge due to the progressive filling of

5478-446: The principal ores of cerium and the light lanthanides. Enriched deposits of rare-earth elements at the surface of the Earth, carbonatites and pegmatites , are related to alkaline plutonism , an uncommon kind of magmatism that occurs in tectonic settings where there is rifting or that are near subduction zones. In a rift setting, the alkaline magma is produced by very small degrees of partial melting (<1%) of garnet peridotite in

5561-440: The processes at work. The geochemical study of the REE is not carried out on absolute concentrations – as it is usually done with other chemical elements – but on normalized concentrations in order to observe their serial behaviour. In geochemistry, rare-earth elements are typically presented in normalized "spider" diagrams, in which concentration of rare-earth elements are normalized to a reference standard and are then expressed as

5644-421: 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. Some ilmenite concentrates contain small amounts of scandium and other rare-earth elements, which could be analysed by X-ray fluorescence (XRF). Before

5727-420: The rock retains the rare-earth element concentration from its source. Rare-earth mineral The following includes the relatively common hydrothermal rare-earth minerals and minerals that often contain significant rare-earth substitution: This particular group of minerals contains elements that are considered rare in our planet's makeup. To be classified as a rare earth mineral, a thorough examination of

5810-485: The same ore deposits as the lanthanides and exhibit similar chemical properties, but have different electrical and magnetic properties . The term 'rare-earth' is a misnomer because they are not actually scarce, although historically it took a long time to isolate these elements. These metals tarnish slowly in air at room temperature and react slowly with cold water to form hydroxides, liberating hydrogen. They react with steam to form oxides and ignite spontaneously at

5893-576: The seafloor, bit by bit, over tens of millions of years. One square patch of metal-rich mud 2.3 kilometers wide might contain enough rare earths to meet most of the global demand for a year, Japanese geologists report in Nature Geoscience ." "I believe that rare[-]earth resources undersea are much more promising than on-land resources," said Kato. "[C]oncentrations of rare earths were comparable to those found in clays mined in China. Some deposits contained twice as much heavy rare earths such as dysprosium,

5976-487: The sedimentary parent lithology contains REE-bearing, heavy resistate minerals. In 2011, Yasuhiro Kato, a geologist at the University of Tokyo who led a study of Pacific Ocean seabed mud, published results indicating the mud could hold rich concentrations of rare-earth minerals. The deposits, studied at 78 sites, came from "[h]ot plumes from hydrothermal vents pull[ing] these materials out of seawater and deposit[ing] them on

6059-419: The sequential accretion of the Earth, the dense rare-earth elements were incorporated into the deeper portions of the planet. Early differentiation of molten material largely incorporated the rare earths into mantle rocks. The high field strength and large ionic radii of rare earths make them incompatible with the crystal lattices of most rock-forming minerals, so REE will undergo strong partitioning into

6142-497: The series causes chemical variations. Europium is exempt of this classification as it has two valence states: Eu and Eu . Yttrium is grouped as heavy rare-earth element due to chemical similarities. The break between the two groups is sometimes put elsewhere, such as between elements 63 (europium) and 64 (gadolinium). The actual metallic densities of these two groups overlap, with the "light" group having densities from 6.145 (lanthanum) to 7.26 (promethium) or 7.52 (samarium) g/cc, and

6225-401: The southern Ural Mountains was documented by Gustav Rose . The Russian chemist R. Harmann proposed that a new element he called " ilmenium " should be present in this mineral, but later, Christian Wilhelm Blomstrand , Galissard de Marignac, and Heinrich Rose found only tantalum and niobium ( columbium ) in it. The exact number of rare-earth elements that existed was highly unclear, and

6308-766: The subducting plate within the asthenosphere (80 to 200 km depth) produces a volatile-rich magma (high concentrations of CO 2 and water), with high concentrations of alkaline elements, and high element mobility that the rare earths are strongly partitioned into. This melt may also rise along pre-existing fractures, and be emplaced in the crust above the subducting slab or erupted at the surface. REE-enriched deposits forming from these melts are typically S-Type granitoids. Alkaline magmas enriched with rare-earth elements include carbonatites, peralkaline granites (pegmatites), and nepheline syenite . Carbonatites crystallize from CO 2 -rich fluids, which can be produced by partial melting of hydrous-carbonated lherzolite to produce

6391-547: The surface. The most important rare-earth oxide deposit, the Central Lanthanide Deposit, CLD, is located at the center of the carbonatite with the niobium/tantalum and other deposits generally located towards outer fringes. Discovered in 1988, the CLD represents a spectacular enrichment of rare-earth deposit sediments. The deposit is believed to be the largest and highest grade of its type in the world. The Mount Weld deposit

6474-399: The system under examination and the occurring geochemical processes can be obtained. The anomalies represent enrichment (positive anomalies) or depletion (negative anomalies) of specific elements along the series and are graphically recognizable as positive or negative "peaks" along the REE patterns. The anomalies can be numerically quantified as the ratio between the normalized concentration of

6557-479: The time that ion exchange methods and elution were available, the separation of the rare earths was primarily achieved by repeated precipitation or crystallization . In those days, the first separation was into two main groups, the cerium earths (lanthanum, cerium, praseodymium, neodymium, and samarium) and the yttrium earths (scandium, yttrium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium). Europium, gadolinium, and terbium were either considered as

6640-484: The two ores ceria and yttria (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,

6723-400: The weathering process that these minerals require, they are classified as rare earth minerals. In addition to these rare minerals other elements are contained within this soil like substance such as iron and nickel. Thus having a red colour like soil through the oxidation of these minerals. Basalt is the source of laterite, which is a material that contains aluminum. Its high aluminum content

6806-492: Was in fact still a mixture of oxides. In 1842 Mosander also separated the yttria into three oxides: pure yttria, terbia, and erbia (all the names are derived from the town name "Ytterby"). The earth giving pink salts he called terbium ; the one that yielded yellow peroxide he called erbium . In 1842 the number of known rare-earth elements had reached six: yttrium, cerium, lanthanum, didymium, erbium, and terbium. Nils Johan Berlin and Marc Delafontaine tried also to separate

6889-494: Was once thought to be in space group I 2 1 3 (no. 199), but is now known to be in space group Ia 3 (no. 206). The structure is similar to that of fluorite or cerium dioxide (in which the cations form a face-centred cubic lattice and the anions sit inside the tetrahedra of cations), except that one-quarter of the anions (oxygen) are missing. The unit cell of these sesquioxides corresponds to eight unit cells of fluorite or cerium dioxide, with 32 cations instead of 4. This

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