|Standard atomic weight Ar, std(Sc)|||
|Scandium in the periodic table|
|Element category||Transition metal|
|Electron configuration||[Ar] 3d1 4s2|
|Electrons per shell||2, 8, 9, 2|
|Phase at STP||solid|
|Melting point||1814 K (1541 °C, 2806 °F)|
|Boiling point||3109 K (2836 °C, 5136 °F)|
|Density (near r.t.)||2.985 g/cm3|
|when liquid (at m.p.)||2.80 g/cm3|
|Heat of fusion||14.1 kJ/mol|
|Heat of vaporization||332.7 kJ/mol|
|Molar heat capacity||25.52 J/(mol·K)|
|Oxidation states||0, +1, +2,+3 (an amphoteric oxide)|
|Electronegativity||Pauling scale: 1.36|
|Atomic radius||empirical: 162 pm|
|Covalent radius||170±7 pm|
|Van der Waals radius||211 pm|
|Spectral lines of scandium|
|Crystal structure||hexagonal close-packed (hcp)|
|Thermal expansion||?, poly: 10.2 µm/(m·K) (at r.t.)|
|Thermal conductivity||15.8 W/(m·K)|
|Electrical resistivity||?, poly: 562 n?·m (at r.t., calculated)|
|Magnetic susceptibility||+315.0·10-6 cm3/mol (292 K)|
|Young's modulus||74.4 GPa|
|Shear modulus||29.1 GPa|
|Bulk modulus||56.6 GPa|
|Brinell hardness||736-1200 MPa|
|Discovery and first isolation||Lars Fredrik Nilson (1879)|
|Main isotopes of scandium|
Scandium is a chemical element with the symbol Sc and atomic number 21. A silvery-white metallic d-block element, it has historically been classified as a rare-earth element, together with yttrium and the lanthanides. It was discovered in 1879 by spectral analysis of the minerals euxenite and gadolinite from Scandinavia.
Scandium is present in most of the deposits of rare-earth and uranium compounds, but it is extracted from these ores in only a few mines worldwide. Because of the low availability and the difficulties in the preparation of metallic scandium, which was first done in 1937, applications for scandium were not developed until the 1970s, when the positive effects of scandium on aluminium alloys were discovered, and its use in such alloys remains its only major application. The global trade of scandium oxide is 15-20 tonnes per year.
The properties of scandium compounds are intermediate between those of aluminium and yttrium. A diagonal relationship exists between the behavior of magnesium and scandium, just as there is between beryllium and aluminium. In the chemical compounds of the elements in group 3, the predominant oxidation state is +3.
Scandium is a soft metal with a silvery appearance. It develops a slightly yellowish or pinkish cast when oxidized by air. It is susceptible to weathering and dissolves slowly in most dilute acids. It does not react with a 1:1 mixture of nitric acid (HNO3) and 48% hydrofluoric acid (HF), possibly due to the formation of an impermeable passive layer. Scandium turnings ignite in air with a brilliant yellow flame to form scandium oxide.
In nature, scandium is found exclusively as the isotope 45Sc, which has a nuclear spin of 7/2; this is its only stable isotope. Thirteen radioisotopes have been characterized with the most stable being 46Sc, which has a half-life of 83.8 days; 47Sc, 3.35 days; the positron emitter 44Sc, 4 h; and 48Sc, 43.7 hours. All of the remaining radioactive isotopes have half-lives less than 4 hours, and the majority of these have half-lives less than 2 minutes. This element also has five nuclear isomers, with the most stable being 44mSc (t1/2 = 58.6 h).
The isotopes of scandium range from 36Sc to 60Sc. The primary decay mode at masses lower than the only stable isotope, 45Sc, is electron capture, and the primary mode at masses above it is beta emission. The primary decay products at atomic weights below 45Sc are calcium isotopes and the primary products from higher atomic weights are titanium isotopes.
In Earth's crust, scandium is not rare. Estimates vary from 18 to 25 ppm, which is comparable to the abundance of cobalt (20-30 ppm). Scandium is only the 50th most common element on Earth (35th most abundant in the crust), but it is the 23rd most common element in the Sun. However, scandium is distributed sparsely and occurs in trace amounts in many minerals. Rare minerals from Scandinavia and Madagascar such as thortveitite, euxenite, and gadolinite are the only known concentrated sources of this element. Thortveitite can contain up to 45% of scandium in the form of scandium oxide.
The world production of scandium is in the order of 15-20 tonnes per year, in the form of scandium oxide. The demand is about 50% higher, and both the production and demand keep increasing. In 2003, only three mines produced scandium: the uranium and iron mines in Zhovti Vody in Ukraine, the rare-earth mines in Bayan Obo, China, and the apatite mines in the Kola peninsula, Russia; since then many other countries have built scandium-producing facilities, including 5 tonnes/year (7.5 tonnes/year Sc2O3) by Nickel Asia Corporation and Sumitomo Metal Mining in the Philippines. In the United States, NioCorp Development hopes[when?] to raise $1 billion toward opening a niobium mine at its Elk Creek site in southeast Nebraska which may be able to produce as much as 95 tonnes of scandium oxide annually. In each case scandium is a byproduct from the extraction of other elements and is sold as scandium oxide.
Madagascar and the Iveland-Evje region in Norway have the only deposits of minerals with high scandium content, thortveitite (Sc,Y)2(Si2O7) but these are not being exploited. The mineral kolbeckite ScPO4·2H2O has a very high scandium content but is not available in any larger deposits.
The absence of reliable, secure, stable, long-term production has limited the commercial applications of scandium. Despite this low level of use, scandium offers significant benefits. Particularly promising is the strengthening of aluminium alloys with as little as 0.5% scandium. Scandium-stabilized zirconia enjoys a growing market demand for use as a high-efficiency electrolyte in solid oxide fuel cells.
Scandium chemistry is almost completely dominated by the trivalent ion, Sc3+. The radii of M3+ ions in the table below indicate that the chemical properties of scandium ions have more in common with yttrium ions than with aluminium ions. In part because of this similarity, scandium is often classified as a lanthanide-like element.
The halides ScX3, where X= Cl, Br, or I, are very soluble in water, but ScF3 is insoluble. In all four halides, the scandium is 6-coordinated. The halides are Lewis acids; for example, ScF3 dissolves in a solution containing excess fluoride ion to form [ScF6]3-. The coordination number 6 is typical for Sc(III). In the larger Y3+ and La3+ ions, coordination numbers of 8 and 9 are common. Scandium triflate is sometimes used as a Lewis acid catalyst in organic chemistry.
Scandium forms a series of organometallic compounds with cyclopentadienyl ligands (Cp), similar to the behavior of the lanthanides. One example is the chlorine-bridged dimer, [ScCp2Cl]2 and related derivatives of pentamethylcyclopentadienyl ligands.
Compounds that feature scandium in oxidation states other than +3 are rare but well characterized. The blue-black compound CsScCl3 is one of the simplest. This material adopts a sheet-like structure that exhibits extensive bonding between the scandium(II) centers.Scandium hydride is not well understood, although it appears not to be a saline hydride of Sc(II). As is observed for most elements, a diatomic scandium hydride has been observed spectroscopically at high temperatures in the gas phase. Scandium borides and carbides are non-stoichiometric, as is typical for neighboring elements.
Dmitri Mendeleev, who is referred to as the father of the periodic table, predicted the existence of an element ekaboron, with an atomic mass between 40 and 48 in 1869. Lars Fredrik Nilson and his team detected this element in the minerals euxenite and gadolinite in 1879. Nilson prepared 2 grams of scandium oxide of high purity. He named the element scandium, from the Latin Scandia meaning "Scandinavia". Nilson was apparently unaware of Mendeleev's prediction, but Per Teodor Cleve recognized the correspondence and notified Mendeleev.
Metallic scandium was produced for the first time in 1937 by electrolysis of a eutectic mixture of potassium, lithium, and scandium chlorides, at 700-800 °C. The first pound of 99% pure scandium metal was produced in 1960. Production of aluminium alloys began in 1971, following a US patent. Aluminium-scandium alloys were also developed in the USSR.
In early 2018, evidence was gathered from spectrometer data of significant scandium, vanadium and yttrium abundances in red giant stars in the Nuclear Star Cluster (NSC) in the Galactic Center. Further research showed that this was an illusion caused by the relatively low temperature (below 3,500 K) of these stars masking the abundance signals, and that this phenomenon was observable in other red giants.
The addition of scandium to aluminium limits the grain growth in the heat zone of welded aluminium components. This has two beneficial effects: the precipitated Al3Sc forms smaller crystals than in other aluminium alloys, and the volume of precipitate-free zones at the grain boundaries of age-hardening aluminium alloys is reduced. Both of these effects increase the usefulness of the alloy.[why?] However, titanium alloys, which are similar in lightness and strength, are cheaper and much more widely used.
The alloy Al20Li20Mg10Sc20Ti30 is as strong as titanium, light as aluminium, and hard as ceramic.
The main application of scandium by weight is in aluminium-scandium alloys for minor aerospace industry components. These alloys contain between 0.1% and 0.5% of scandium. They were used in the Russian military aircraft, specifically the Mikoyan-Gurevich MiG-21 and MiG-29.
Some items of sports equipment, which rely on high-performance materials, have been made with scandium-aluminium alloys, including baseball bats and bicycle frames and components.Lacrosse sticks are also made with scandium. The American firearm manufacturing company Smith & Wesson produces semi-automatic pistols and revolvers with frames of scandium alloy and cylinders of titanium or carbon steel.
Dentists use erbium-chromium-doped yttrium-scandium-gallium garnet (Er,Cr:YSGG) lasers for cavity preparation and in endodontics.
The first scandium-based metal-halide lamps were patented by General Electric and initially made in North America, although they are now produced in all major industrialized countries. Approximately 20 kg of scandium (as Sc2O3) is used annually in the United States for high-intensity discharge lamps. One type of metal-halide lamp, similar to the mercury-vapor lamp, is made from scandium triiodide and sodium iodide. This lamp is a white-light source with high color rendering index that sufficiently resembles sunlight to allow good color-reproduction with TV cameras. About 80 kg of scandium is used in metal-halide lamps/light bulbs globally per year.
Elemental scandium is considered non-toxic, though extensive animal testing of scandium compounds has not been done. The median lethal dose (LD50) levels for scandium chloride for rats have been determined as 755 mg/kg for intraperitoneal and 4 g/kg for oral administration. In the light of these results, compounds of scandium should be handled as compounds of moderate toxicity.