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==History==
==History==
In 1871, existence of gallium was first predicted by Russian chemist [[Dmitri Mendeleev]], who named it "[[Mendeleev's predicted elements|eka-aluminium]]" on the basis of its position in his [[periodic table]]. He also predicted several properties of the element, which correspond closely to real gallium properties, such as [[density]], [[melting point]], oxide character and bonding in chloride.<ref>{{cite book|title=The Ingredients: A Guided Tour of the Elements|author=Ball, Philip|publisher=Oxford University Press|page=105|year=2002|isbn=0-19-284100-9}}</ref>
In 1871, existence of gallium was first predicted by Russian chemist [http://www.fimfiction.net/user/Aperture%20lemon Aperture lemon], who named it "[[Mendeleev's predicted elements|eka-aluminium]]" on the basis of its position in his [[periodic table]]. He also predicted several properties of the element, which correspond closely to real gallium properties, such as [[density]], [[melting point]], oxide character and bonding in chloride.<ref>{{cite book|title=The Ingredients: A Guided Tour of the Elements|author=Ball, Philip|publisher=Oxford University Press|page=105|year=2002|isbn=0-19-284100-9}}</ref>


Gallium was discovered [[spectroscopy|spectroscopically]] by French chemist [[Paul Emile Lecoq de Boisbaudran]] in 1875 by its characteristic spectrum (two [[violet (color)|violet]] lines) in an examination of a [[sphalerite]] sample.<ref name="Bois">{{Cite journal|title = Caractères chimiques et spectroscopiques d'un nouveau métal, le gallium, découvert dans une blende de la mine de Pierrefitte, vallée d'Argelès (Pyrénées)| first = Lecoq |last = de Boisbaudran |page=493|journal = Comptes rendus|volume = 81|url = http://gallica.bnf.fr/ark:/12148/bpt6k3038w/f490.table|accessdate = 2008-09-23|date = 1835-1965}}</ref> <!--{{doi|10.1002/andp.18762351216}}--> Later that year, Lecoq obtained the free metal by [[electrolysis]] of its [[hydroxide]] in [[potassium hydroxide]] solution. He named the element "gallia", from [[Latin]] ''Gallia'' meaning [[Gaul]], after his native land of France. It was later claimed that, in one of those multilingual [[pun]]s so beloved of men of science in the 19th century, he had also named gallium after himself, as his name, "Le coq", is the French for "the [[rooster]]", and the [[Latin]] for "rooster" is "''gallus''"; however, in an 1877 article Lecoq denied this supposition.<ref name="Weeks">{{Cite journal|title = The discovery of the elements. XIII. Some elements predicted by Mendeleeff |pages = 1605–1619|last = Weeks|first = Mary Elvira |authorlink=Mary Elvira Weeks|doi=10.1021/ed009p1605|journal = [[Journal of Chemical Education]] |volume =9 |issue =9 |year = 1932|bibcode = 1932JChEd...9.1605W }}</ref> (Cf. the naming of the [[J/ψ meson#The name|J/ψ meson]] and the dwarf planet [[Pluto]].)
Gallium was discovered [[spectroscopy|spectroscopically]] by French chemist [http://www.fimfiction.net/user/Ethesto+the+Pony+Butcher Ethesto] in 1875 by its characteristic spectrum (two [[violet (color)|violet]] lines) in an examination of a [[sphalerite]] sample.<ref name="Bois">{{Cite journal|title = Caractères chimiques et spectroscopiques d'un nouveau métal, le gallium, découvert dans une blende de la mine de Pierrefitte, vallée d'Argelès (Pyrénées)| first = Lecoq |last = de Boisbaudran |page=493|journal = Comptes rendus|volume = 81|url = http://gallica.bnf.fr/ark:/12148/bpt6k3038w/f490.table|accessdate = 2008-09-23|date = 1835-1965}}</ref> <!--{{doi|10.1002/andp.18762351216}}--> Later that year, Lecoq obtained the free metal by [[electrolysis]] of its [[hydroxide]] in [[potassium hydroxide]] solution. He named the element "gallia", from [[Latin]] ''Gallia'' meaning [[Gaul]], after his native land of France. It was later claimed that, in one of those multilingual [[pun]]s so beloved of men of science in the 19th century, he had also named gallium after himself, as his name, "Le coq", is the French for "the [[rooster]]", and the [[Latin]] for "rooster" is "''gallus''"; however, in an 1877 article Lecoq denied this supposition.<ref name="Weeks">{{Cite journal|title = The discovery of the elements. XIII. Some elements predicted by Mendeleeff |pages = 1605–1619|last = Weeks|first = Mary Elvira |authorlink=Mary Elvira Weeks|doi=10.1021/ed009p1605|journal = [[Journal of Chemical Education]] |volume =9 |issue =9 |year = 1932|bibcode = 1932JChEd...9.1605W }}</ref> (Cf. the naming of the [[J/ψ meson#The name|J/ψ meson]] and the dwarf planet [[Pluto]].)


From its discovery in 1875 up to the era of semiconductors, its primary uses were in high-temperature thermometric applications and in preparation of metal alloys with unusual properties of stability, or ease of melting; some being liquid at room temperature or below. The development of gallium arsenide as a direct band gap semiconductor in the 1960s ushered in the most important stage in the applications of gallium.
From its discovery in 1875 up to the era of semiconductors, its primary uses were in high-temperature thermometric applications and in preparation of metal alloys with unusual properties of stability, or ease of melting; some being liquid at room temperature or below. The development of gallium arsenide as a direct band gap semiconductor in the 1960s ushered in the most important stage in the applications of gallium.

Revision as of 03:29, 26 November 2013

Template:Distinguish2

This article is about the chemical element. For other uses, see Gallium (disambiguation).
Gallium, 31Ga
Gallium
Pronunciation/ˈɡæliəm/ ​(GAL-ee-əm)
Appearancesilvery blue
Standard atomic weight Ar°(Ga)
Gallium in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
Al
↑
Ga
↓
In
zinc ← gallium → germanium
Atomic number (Z)31
Groupgroup 13 (boron group)
Periodperiod 4
Block  p-block
Electron configuration[Ar] 3d10 4s2 4p1
Electrons per shell2, 8, 18, 3
Physical properties
Phase at STPsolid
Melting point302.9146 K ​(29.7646 °C, ​85.5763 °F)
Boiling point2676 K ​(2403 °C, ​4357 °F)[3][4]
Density (at 20° C)5.907 g/cm3[5]
when liquid (at m.p.)6.095 g/cm3
Heat of fusion5.59 kJ/mol
Heat of vaporization256 kJ/mol[3]
Molar heat capacity25.86 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1310 1448 1620 1838 2125 2518
Atomic properties
Oxidation states−5, −4, −3,[6] −2, −1, 0, +1, +2, +3[7] (an amphoteric oxide)
ElectronegativityPauling scale: 1.81
Ionization energies
  • 1st: 578.8 kJ/mol
  • 2nd: 1979.3 kJ/mol
  • 3rd: 2963 kJ/mol
  • (more)
Atomic radiusempirical: 135 pm
Covalent radius122±3 pm
Van der Waals radius187 pm
Color lines in a spectral range
Spectral lines of gallium
Other properties
Natural occurrenceprimordial
Crystal structure ​base-centered orthorhombic (oS8)
Lattice constants
Base-centered orthorhombic crystal structure for gallium
a = 452.05 pm
b = 766.25 pm
c = 452.66 pm (at 20 °C)[5]
Thermal expansion20.5×10−6/K (at 20 °C)[5][a]
Thermal conductivity40.6 W/(m⋅K)
Electrical resistivity270 nΩ⋅m (at 20 °C)
Magnetic orderingdiamagnetic
Molar magnetic susceptibility−21.6×10−6 cm3/mol (at 290 K)[8]
Young's modulus9.8 GPa
Speed of sound thin rod2740 m/s (at 20 °C)
Poisson ratio0.47
Mohs hardness1.5
Brinell hardness56.8–68.7 MPa
CAS Number7440-55-3
History
Namingafter Gallia (Latin for: France), homeland of the discoverer
PredictionDmitri Mendeleev (1871)
Discovery and first isolationLecoq de Boisbaudran (1875)
Isotopes of gallium
Main isotopes[9] Decay
abun­dance half-life (t1/2) mode pro­duct
66Ga synth 9.5 h β+ 66Zn
67Ga synth 3.3 d ε 67Zn
68Ga synth 1.2 h β+ 68Zn
69Ga 60.1% stable
70Ga synth 21 min β− 70Ge
ε 70Zn
71Ga 39.9% stable
72Ga synth 14.1 h β− 72Ge
73Ga synth 4.9 h β− 73Ge
 Category: Gallium
| references

Gallium is a chemical element with symbol Ga and atomic number 31. Elemental gallium does not occur in free form in nature, but as the gallium(III) compounds that are in trace amounts in zinc ores and in bauxite. Gallium is a soft silvery metal, and elemental gallium is a brittle solid at low temperatures. If it is held in the human hand long enough, gallium will melt, since it melts at the temperature of about 29.76 °C (85.57 °F) (slightly above room temperature). The melting point of gallium is used as a temperature reference point. The alloy galinstan (68.5% gallium, 21.5% indium, and 10% tin) has the even lower melting point of −19 °C (−2 °F), well below the freezing point of water. Beginning with its discovery in 1875 through the era of semiconductors, gallium was used primarily as an agent to make alloys that melt at low temperatures. Then, gallium became useful in semiconductors, including as a dopant.

Today, nearly all gallium is used in electronics. Gallium arsenide, the primary chemical compound of gallium in electronics, is used in microwave circuits, high-speed switching circuits, and infrared circuits. Gallium nitride and indium gallium nitride, minority semiconductor uses, produce blue and violet light-emitting diodes (LEDs) and diode lasers.

Gallium has no known role in biology. Because gallium(III) and ferric salts behave similarly in biological systems, gallium ions often mimic iron ions in medical applications. Some pharmaceuticals containing gallium and radiopharmaceuticals have been used rarely.

Physical properties

Crystallization of gallium from the melt

Elemental gallium is not found in nature, but it is easily obtained by smelting. Very pure gallium metal has a brilliant silvery color and its solid metal fractures conchoidally like glass. Gallium metal expands by 3.1% when it solidifies, and therefore storage in either glass or metal containers is avoided, due to the possibility of container rupture with freezing. Gallium shares the higher-density liquid state with only a few materials like silicon, germanium, bismuth and water.

Gallium attacks most other metals by diffusing into their metal lattice. Gallium, for example, diffuses into the grain boundaries of aluminium-zinc alloys[10] or steel,[11] making them very brittle. Gallium easily alloys with many metals, and is used in small quantities as a plutonium-gallium alloy in the plutonium cores of nuclear bombs, to help stabilize the plutonium crystal structure.[12]

The melting point of 302.9146 K (29.7646 °C, 85.5763 °F) is near room temperature. Gallium's melting point (mp) is one of the formal temperature reference points in the International Temperature Scale of 1990 (ITS-90) established by BIPM.[13][14][15] The triple point of gallium of 302.9166 K (29.7666 °C, 85.5799 °F), is being used by NIST in preference to gallium's melting point.[16]

The unique melting point of gallium allows it to melt in one's hand, and then refreeze if removed. This metal has a strong tendency to supercool below its melting point/freezing point. Seeding with a crystal helps to initiate freezing. Gallium is one of the metals (with caesium, rubidium, mercury and likely francium) that are liquid at or near-normal room temperature, and can therefore be used in metal-in-glass high-temperature thermometers. It is also notable for having one of the largest liquid ranges for a metal, and (unlike mercury) for having a low vapor pressure at high temperatures. Gallium's boiling point, 2477 K, is more than eight times higher than its melting point on the absolute scale, making it the greatest ratio between melting point and boiling point of any element. Unlike mercury, liquid gallium metal wets glass and skin, making it mechanically more difficult to handle (even though it is substantially less toxic and requires far fewer precautions). For this reason as well as the metal contamination and freezing-expansion problems, samples of gallium metal are usually supplied in polyethylene packets within other containers.

Properties of Ga for different crystal axes[17]
Property a b c
α (~25 °C, µm/m) 16 11 31
ρ (29.7 °C, nΩ·m) 543 174 81
ρ (0 °C, nΩ·m) 480 154 71.6
ρ (77 K, nΩ·m) 101 30.8 14.3
ρ (4.2 K, pΩ·m) 13.8 6.8 1.6

Gallium does not crystallize in any of the simple crystal structures. The stable phase under normal conditions is orthorhombic with 8 atoms in the conventional unit cell. Each atom has only one nearest neighbor (at a distance of 244 pm) and six other neighbors within additional 39 pm. Many stable and metastable phases are found as function of temperature and pressure.

The bonding between the two nearest neighbors is covalent, hence Ga2 dimers are seen as the fundamental building blocks of the crystal. This explains the drop of the melting point compared to its neighbor elements aluminium and indium.

The physical properties of gallium are highly anisotropic, i.e. have different values along the three major crystallographical axes a, b and c (see table); for this reason, there is a significant difference between the linear (α) and volume thermal expansion coefficients. The properties of gallium are also strongly temperature-dependent, especially near the melting point. For example, the thermal expansion coefficient increases by several hundred percent upon melting.[17]

Chemical properties

See also: Category:Gallium compounds

Gallium is found primarily in the +3 oxidation state. The +1 oxidation is also attested in some compounds, although they tend to disproportionate into elemental gallium and gallium(III) compounds. What are sometimes referred to as gallium(II) compounds are actually mixed-oxidation state compounds containing both gallium(I) and gallium(III).[18]

Chalcogen compounds

Gallium reacts with chalcogen elements (sometimes called the "oxygen family") only at relatively high temperatures. At room temperature, gallium metal is unreactive towards air and water due to the formation of a passive, protective oxide layer. At higher temperatures, however, it reacts with oxygen in the air to form gallium(III) oxide, Ga
2O
3.[18] Reducing Ga
2O
3 with elemental gallium in vacuum at 500 °C to 700 °C yields the dark brown gallium(I) oxide, Ga
2O.[19]: 285  Ga
2O is a very strong reducing agent, capable of reducing H
2SO
4 to H
2S.[19]: 207  It disproportionates at 800 °C back to gallium and Ga
2O
3.[20]

Gallium sulfide, Ga
2S
3, has 3 possible crystal modifications.[20]: 104  It can be made by the reaction of gallium with hydrogen sulfide (H
2S) at 950 °C.[19]: 162  Alternatively, Ga(OH)
3 can also be used at 747 °C:[21]

2 Ga(OH)
3 + 3 H
2S → Ga
2S
3 + 6 H
2O

Reacting a mixture of alkali metal carbonates and Ga
2O
3 with H
2S leads to the formation of thiogallates containing the [Ga
2S
4]2−
 anion. Strong acids decompose these salts, releasing H
2S in the process.[20]: 104–105  The mercury salt, HgGa
2S
4, can be used as a phosphor.[22]

Gallium also forms sulfides in lower oxidation states, such as gallium(II) sulfide and the green gallium(I) sulfide, the latter of which is produced from the former by heating to 1000 °C under a stream of nitrogen.[20]: 94 

The other binary chalcogenides, Ga
2Se
3 and Ga
2Te
3, have zincblende structure. They are all semiconductors, but are easily hydrolysed, limiting their usefulness.[20]: 104 

Aqueous chemistry

Strong acids dissolve gallium, forming gallium(III) salts such as Ga
2(SO
4)
3 and Ga(NO
3)
3. Aqueous solutions of gallium(III) salts contain the hydrated gallium ion, [Ga(H
2O)
6]3+
.[23]: 1033  Gallium(III) hydroxide, Ga(OH)
3, may be precipitated from gallium(III) solutions by adding ammonia. Dehydrating Ga(OH)
3 at 100 °C produces gallium oxide hydroxide, GaO(OH).[19]: 140–141 

Alkaline hydroxide solutions dissolve gallium, forming gallate salts containing the Ga(OH)−
4 anion.[18][23]: 1033 [24] Gallium hydroxide, which is amphoteric, also dissolves in alkali to form gallate salts.[19]: 141  Although earlier work suggested Ga(OH)3−
6 as another possible gallate anion,[25] this species was not found in later work.[24]

Pnictogen compounds

Gallium reacts with ammonia at 1050 °C to form gallium nitride, GaN. Gallium also forms binary compounds with phosphorus, arsenic, and antimony: gallium phosphide (GaP), gallium arsenide (GaAs), and gallium antimonide (GaSb). These compounds have the same structure as ZnS, and have important semiconducting properties.[23]: 1034  GaP, GaAs, and GaSb can be synthesized by the direct reaction of gallium with elemental phosphorus, arsenic, or antimony.[20]: 99  They exhibit higher electrical conductivity than GaN.[20]: 101  GaP can also be synthesized by the reaction of Ga
2O with phosphorus at low temperatures.[26]

Gallium also forms ternary nitrides; for example:[20]: 99 

Li
3Ga + N
2 → Li
3GaN
2

Similar compounds with phosphorus and arsenic also exist: Li
3GaP
2 and Li
3GaAs
2. These compounds are easily hydrolyzed by dilute acids and water.[20]: 101 

Halides

See also: Gallium halides

Gallium(III) oxide reacts with fluorinating agents such as HF or F
2 to form gallium(III) fluoride, GaF
3. It is an ionic compound strongly insoluble in water. However, it does dissolve in hydrofluoric acid, in which it forms an adduct with water, GaF
3·3H
2O. Attempting to dehydrate this adduct instead forms GaF
2OH·nH
2O. The adduct reacts with ammonia to form GaF
3·3NH
3, which can then be heated to form anhydrous GaF
3.[19]: 128–129 

Gallium trichloride is formed by the reaction of gallium metal with chlorine gas.[18] Unlike the trifluoride, gallium(III) chloride exists as dimeric molecules, Ga
2Cl
6, with a melting point of 78 °C. This is also the case for the bromide and iodide, Ga
2Br
6 and Ga
2I
6.[19]: 133 

Like the other group 13 trihalides, gallium(III) halides are Lewis acids, reacting as halide acceptors with alkali metal halides to form salts containing GaX−
4 anions, where X is a halogen. They also react with alkyl halides to form carbocations and GaX−
4.[19]: 136–137 

When heated to a high temperature, gallium(III) halides react with elemental gallium to form the respective gallium(I) halides. For example, GaCl
3 reacts with Ga to form GaCl:

2 Ga + GaCl
3 ⇌ 3 GaCl (g)

At lower temperatures, the equilibrium shifts toward the left and GaCl disproportionates back to elemental gallium and GaCl
3. GaCl can also be made by the reaction of Ga with HCl at 950 °C; it can then be condensed as red solid.[23]: 1036 

Gallium(I) compounds can be stabilized by forming adducts with Lewis acids. For example:

GaCl + AlCl
3 → Ga+
[AlCl
4]−

The so-called "gallium(II) halides", GaX
2, are actually adducts of gallium(I) halides with the respective gallium(III) halides, having the structure Ga+
[GaX
4]−
. For example:[18][23]: 1036 [27]

GaCl + GaCl
3 → Ga+
[GaCl
4]−

Hydrogen compounds

Like aluminium, gallium also forms a hydride, GaH
3, known as gallane, which may be obtained by the reaction of lithium gallanate (LiGaH
4) with gallium(III) chloride at −30 °C:[23]: 1031 

3 LiGaH
4 + GaCl
3 → 3 LiCl + 4 GaH
3

In the presence of dimethyl ether as solvent, GaH
3 polymerizes to (GaH
3)
n. If no solvent is used, the dimer Ga
2H
6 (digallane) is formed as a gas. Its structure is similar to diborane, having two hydrogen atoms bridging the two gallium centers,[23]: 1031  unlike α-AlH
3 in which aluminium has a coordination number of 6.[23]: 1008 

Gallane is unstable above −10 °C, decomposing to elemental gallium and hydrogen.[28]

History

In 1871, existence of gallium was first predicted by Russian chemist Aperture lemon, who named it "eka-aluminium" on the basis of its position in his periodic table. He also predicted several properties of the element, which correspond closely to real gallium properties, such as density, melting point, oxide character and bonding in chloride.[29]

Gallium was discovered spectroscopically by French chemist Ethesto in 1875 by its characteristic spectrum (two violet lines) in an examination of a sphalerite sample.[30] Later that year, Lecoq obtained the free metal by electrolysis of its hydroxide in potassium hydroxide solution. He named the element "gallia", from Latin Gallia meaning Gaul, after his native land of France. It was later claimed that, in one of those multilingual puns so beloved of men of science in the 19th century, he had also named gallium after himself, as his name, "Le coq", is the French for "the rooster", and the Latin for "rooster" is "gallus"; however, in an 1877 article Lecoq denied this supposition.[31] (Cf. the naming of the J/ψ meson and the dwarf planet Pluto.)

From its discovery in 1875 up to the era of semiconductors, its primary uses were in high-temperature thermometric applications and in preparation of metal alloys with unusual properties of stability, or ease of melting; some being liquid at room temperature or below. The development of gallium arsenide as a direct band gap semiconductor in the 1960s ushered in the most important stage in the applications of gallium.

Occurrence

Gallium does not exist in free form in nature, and the few high-gallium minerals such as gallite (CuGaS2) are too rare to serve as a primary source of the element or its compounds. Its abundance in the Earth's crust is approximately 16.9 ppm.[32] Gallium is found and extracted as a trace component in bauxite and to a small extent from sphalerite. The amount extracted from coal, diaspore and germanite in which gallium is also present is negligible. The United States Geological Survey (USGS) estimates gallium reserves to exceed 1 million tonnes, based on 50 ppm by weight concentration in known reserves of bauxite and zinc ores.[33][34] Some flue dusts from burning coal have been shown to contain small quantities of gallium, typically less than 1% by weight.[35][36][37][38]

Production

99.9999% (6N) gallium sealed in vacuum ampoule.

Gallium is a byproduct of the production of aluminium and zinc, whereas the sphalerite for zinc production is the minor source. Most gallium is extracted from the crude aluminium hydroxide solution of the Bayer process for producing alumina and aluminium. A mercury cell electrolysis and hydrolysis of the amalgam with sodium hydroxide leads to sodium gallate. Electrolysis then gives gallium metal. For semiconductor use, further purification is carried out using zone melting, or else single crystal extraction from a melt (Czochralski process). Purities of 99.9999% are routinely achieved and commercially widely available.[39]

In 1986, the production was estimated at 40 tons.[40] In 2007 the production of gallium was 184 tonnes with less than 100 tonnes from mining and the rest from scrap recycling.[33] By 2011 world production of gallium was an estimated 216 metric tons.[41]

Applications

The semiconductor applications dominate the commercial use of gallium, accounting for 98% of applications. The next major application is for gadolinium gallium garnets.[40]

Semiconductors

Gallium-based blue LEDs

Because of this application, extremely high-purity (99.9999+%) gallium is commercially available. Gallium arsenide (GaAs) and gallium nitride (GaN) used in electronic components represented about 98% of the gallium consumption in the United States in 2007. About 66% of semiconductor gallium is used in the U.S. in integrated circuits (mostly gallium arsenide), such as the manufacture of ultra-high speed logic chips and MESFETs for low-noise microwave preamplifiers in cell phones. About 20% is used in optoelectronics.[33] Worldwide, gallium arsenide makes up 95% of the annual global gallium consumption.[39]

Gallium arsenide is used in optoelectronics in a variety of infrared applications. Aluminium gallium arsenide (AlGaAs) is used in high-powered infrared laser diodes. As a component of the semiconductors indium gallium nitride and gallium nitride, gallium is used to produce blue and violet optoelectronic devices, mostly laser diodes and light-emitting diodes. For example, gallium nitride 405 nm diode lasers are used as a violet light source for higher-density compact disc data storage, in the Blu-ray Disc standard.[42]

Multijunction photovoltaic cells, developed for satellite power applications, are made by molecular beam epitaxy or metalorganic vapour phase epitaxy of thin films of gallium arsenide, indium gallium phosphide or indium gallium arsenide.The Mars Exploration Rovers and several satellites use triple junction gallium arsenide on germanium cells.[43] Gallium is also a component in photovoltaic compounds (such as copper indium gallium selenium sulfide or Cu(In,Ga)(Se,S)2) for use in solar panels as a cost-efficient alternative to crystalline silicon.[44]

Galinstan and other alloys

Gallium readily alloys with most metals, and has been used as a component in low-melting alloys. A nearly eutectic alloy of gallium, indium, and tin is a room temperature liquid that is available in medical thermometers. This alloy, with the trade-name Galinstan (with the "-stan" referring to the tin), has a low freezing point of −19 °C (−2.2 °F).[45] It has been suggested that this family of alloys could also be used to cool computer chips in place of water.[46] Gallium alloys have been evaluated as substitutes for mercury dental amalgams, but these materials have yet to see wide acceptance.

Because gallium wets glass or porcelain, gallium can be used to create brilliant mirrors. When the wetting action of gallium-alloys is not desired (as in Galinstan glass thermometers), the glass must be protected with a transparent layer of gallium(III) oxide.[47]

The plutonium used in nuclear weapon pits is machined by alloying with gallium to stabilize its δ phase.[48]

Gallium added in quantities up to 2% in common solders can aid wetting and flow characteristics.

Alloys of Al and Ga have been evaluated for hydrogen production.[49]

It is used as the alloying element in the magnetic shape-memory alloy Ni-Mn-Ga.

Biomedical applications

Although gallium has no known role in biology, it mimics iron(III), the gallium ion localizes to and interacts with many processes in the body in which iron(III) is manipulated. As these processes include inflammation, which is a marker for many disease states, several gallium salts are used, or are in development, as both pharmaceuticals and radiopharmaceuticals in medicine. When gallium ions are mistakenly taken up by bacteria such as Pseudomonas, the bacteria's ability to respire is interfered with and the bacteria die. The mechanism behind this is that iron is redox active, which allows for the transfer of electrons during respiration, but gallium is redox inactive.[50][51]

Gallium nitrate (brand name Ganite) has been used as an intravenous pharmaceutical to treat hypercalcemia associated with tumor metastasis to bones. Gallium is thought to interfere with osteoclast function. It may be effective when other treatments for maligancy-associated hypercalcemia are not.[52]

  • Gallium maltolate, an orally absorbable form of gallium(III) ion, is in clinical and preclinical trials as a potential treatment for a number of types of cancer, infectious disease, and inflammatory disease.[53]

A complex amine-phenol Ga(III) compound MR045 was found to be selectively toxic to parasites that have developed resistance to chloroquine, a common drug against malaria. Both the Ga(III) complex and chloroquine act by inhibiting crystallization of hemozoin, a disposal product formed from the digestion of blood by the parasites.[54][55]

Radiogallium salts

Gallium-67 salts such as gallium citrate and gallium nitrate are used as radiopharmaceutical agents in a nuclear medicine imaging procedure commonly referred to as a gallium scan. The form or salt of gallium is unimportant. For these applications, the radioactive isotope 67Ga is used. The body handles Ga3+ in many ways as though it were iron, and thus it is bound (and concentrates) in areas of inflammation, such as infection, and also areas of rapid cell division. This allows such sites to be imaged by nuclear scan techniques. This use has largely been replaced by fluorodeoxyglucose (FDG) for positron emission tomography, "PET" scan and indium-111 labelled leukocyte scans. However, the localization of gallium in the body has some properties which make it unique in some circumstances from competing modalities using other radioisotopes.

Gallium-68, a positron emitter with a half life of 68 min, is now used as a diagnostic radionuclide in PET-CT when linked to pharmaceutical preparations such as DOTATOC, a somatostatin analogue used for neuroendocrine tumors investigation, and DOTA-TATE, a newer one, used for neuroendocrine metastasis and lung neuroendocrine cancer, such as certain types of microcytoma. Gallium-68's preparation as a pharmaceutical is chemical and the radionuclide is extracted by elution from germanium-68, a synthetic radioisotope of germanium, in gallium-68 generators.

Other uses

  • Magnesium gallate containing impurities (such as Mn2+), is beginning to be used in ultraviolet-activated phosphor powder.
  • Neutrino detection. Possibly the largest amount of pure gallium ever collected in a single spot is the Gallium-Germanium Neutrino Telescope used by the SAGE experiment at the Baksan Neutrino Observatory in Russia. This detector contains 55–57 tonnes of liquid gallium.[56] Another experiment was the GALLEX neutrino detector operated in the early 1990s in an Italian mountain tunnel. The detector contained 12.2 tons of watered gallium-71. Solar neutrinos caused a few atoms of 71Ga to become radioactive 71Ge, which were detected. The solar neutrino flux deduced was found to have a deficit of 40% from theory. This was not explained until better solar neutrino detectors and theories were constructed (see SNO).[57]
  • As a liquid metal ion source for a focused ion beam. For example, a focused-gallium-ion beam was used to create the world's smallest book, Teeny Ted from Turnip Town.
  • In a classic prank, scientists would fashion gallium spoons and serve tea to unsuspecting guests. The spoons melt in the hot tea.[58]
  • As an additive in glide wax for skiis, and other low friction surface materials. US 5069803, Sugimura, Kentaro; Hasimoto, Shoji & Ono, Takayuki, "Use of a synthetic resin composition containing gallium particles in the glide surfacing material of skis and other applications", issued 1995 

Precautions

The Ga(III) ion of soluble gallium salts tends to form the insoluble hydroxide when injected in large amounts, and in animals precipitation of this has resulted in renal toxicity. In lower doses, soluble gallium is tolerated well, and does not accumulate as a poison.

While metallic gallium is not considered toxic, the data are inconclusive. Some sources suggest that it may cause dermatitis from prolonged exposure; other tests have not caused a positive reaction. Like most metals, finely divided gallium loses its luster and powdered gallium appears gray. Thus, when gallium is handled with bare hands, the extremely fine dispersion of liquid gallium droplets, which results from wetting skin with the metal, may appear as a gray skin stain.[citation needed]

See also

References

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External links

Wikisource has the text of the 1911 Encyclopædia Britannica article "Gallium".

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