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Gallium

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Template:Distinguish2

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
zincgalliumgermanium
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 structurebase-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 (Template:PronEng) is a chemical element that has the symbol Ga and atomic number 31. A soft silvery metallic poor metal, gallium is a brittle solid at low temperatures but liquefies slightly above room temperature and will melt in the hand. It occurs in trace amounts in bauxite and zinc ores. An important application is in the compounds gallium nitride and gallium arsenide, used as a semiconductor, most notably in light-emitting diodes (LEDs).

Notable characteristics

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 percent 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 germanium, bismuth, antimony and water.

Gallium also attacks most other metals by diffusing into their metal lattice. Gallium for example diffuses into the grain boundaries of Al/Zn alloys[10] or steel.[11], making them very brittle. Also, gallium metal easily alloys with many metals,[citation needed] and was used in small quantities in the core of the first atomic bomb to help stabilize the plutonium crystal structure.[12]

The melting point temperature of 29.76 °C allows the metal to be melted in one's hand. This metal has a strong tendency to supercool below its melting point/freezing point, thus necessitating seeding in order to solidify. Gallium is one of the metals (with caesium, rubidium, francium and mercury) which 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. 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 problem and freezing-expansion problems noted above, samples of gallium metal are usually supplied in polyethylene packets within other containers.

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 nearest neighbors is found to be of covalent character, hence Ga2 dimers are seen as the fundamental building blocks of the crystal. The compound with arsenic, gallium arsenide is a semiconductor commonly used in light-emitting diodes.

High-purity gallium is dissolved slowly by mineral acids.

Gallium has no known biological role, although it might be involved in metabolism stimulation. [13]

History

Gallium (the Latin Gallia means "Gaul," essentially modern France; and the Latin gallus means "rooster") was discovered spectroscopically by Lecoq de Boisbaudran in 1875 by its characteristic spectrum (two violet lines) in an examination of a zinc blende from the Pyrenees. Before its discovery, most of its properties had been predicted and described by Dmitri Mendeleev (who had called the hypothetical element "eka-aluminium") on the basis of its position in his periodic table. Later, in 1875, Boisbaudran obtained the free metal by electrolysis of its hydroxide in potassium hydroxide solution. He named the element "gallia" 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 early 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 Le coq denied this supposition.

Occurrence

Gallium does not exist in free form in nature, nor do any high-gallium minerals exist to serve as a primary source of extraction of the element or its compounds. Gallium is found and extracted as a trace component in bauxite, coal, diaspore, germanite, and sphalerite. The United States Geological Survey (USGS) estimates gallium reserves based on 50 ppm by weight concentration in known reserves of bauxite and zinc ores. Some flue dusts from burning coal have been shown to contain small quantities of gallium, typically less than 1 % by weight.[14][15][16][17]

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.

One chemist estimated in 2007 that at the current rate of usage, the world's supply of gallium would be exhausted by about the year 2017.[18]

Applications

Semiconductor and electronic industry. The semiconductor applications are the main reason for the low-cost commercial availability of the extremely high-purity (99.9999+%) metal:

As a wetting, and alloy improvement agent:

As part of an energy storage mechanism:

  • Aluminium is reactive enough to reduce water to hydrogen, being oxidized to aluminium oxide. However, the aluminium oxide forms a protective coat which prevents further reaction. When gallium is alloyed with aluminium, the coat does not form, thus the alloy can potentially provide a solid hydrogen source for transportation purposes, which would be more convenient than a pressurized hydrogen tank. Resmelting the resultant aluminium oxide and gallium mixture to metallic aluminium and gallium and reforming these into electrodes would constitute most of the energy input into the system, while electricity produced by a hydrogen fuel cell could constitute an energy output.[19][20]The thermodynamic efficiency of the aluminium smelting process is said to be approximately 50 percent.[citation needed] Therefore, at most no more than half the energy that goes into smelting aluminium could be recovered by a fuel cell.

For liquid alloys:

  • It has been suggested that a liquid gallium-tin alloy could be used to cool computer chips in place of water. As it conducts heat approximately 65 times better than water it can make a comparable coolant. [1]
  • Gallium is used in some high temperature thermometers.
  • A liquid Gallium-Indium-Tin alloy has been used in activating Aluminum. Activated Aluminum reacts with water generating Hydrogen and steam. This reaction is considered a feasible process in the hydrogen economy.

Biomedical applications:

  • A low temperature liquid eutectic alloy of gallium, indium, and tin, is widely available in medical thermometers (fever thermometers), replacing problematic mercury. This alloy, with the trade name Galinstan (with the "-stan" referring to the tin), has a freezing point of −20°C.
  • Gallium salts such as gallium citrate and gallium nitrate are used as radiopharmaceutical agents in nuclear medicine imaging. (The form or salt is not important, since it is the free dissolved gallium ion Ga3+ which is active). For these applications, a radioactive isotope such as 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. See gallium scan. This use has largely been replaced by fluorodeoxyglucose (FDG) for positron emission tomography, "PET" scan.
  • Gallium nitrate, both oral and topical, is finding use in treating arthritis.[21]
  • Gallium maltolate is in clinical and preclinical trials as a potential treatment for cancer, infectious disease, and inflammatory disease. [22]
  • Much research is being devoted to gallium alloys as substitutes for mercury dental amalgams, but these compounds have yet to see wide acceptance.
  • Research is being conducted to determine whether gallium can be used to fight bacterial infections in people with cystic fibrosis. Gallium is similar in size to iron, an essential nutrient for respiration. When gallium is mistakenly picked 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. [23][24]

Miscellaneous:

  • 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 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 Ga-71 to become radioactive Ge-71, 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).[2]
  • As a liquid metal ion source for a focused ion beam.

Precautions

While not considered toxic, the data about gallium 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. Powdered gallium appears grey. 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 grey skin stain.

See also

References

  1. ^ "Standard Atomic Weights: Gallium". CIAAW. 1987.
  2. ^ Prohaska, Thomas; Irrgeher, Johanna; Benefield, Jacqueline; Böhlke, John K.; Chesson, Lesley A.; Coplen, Tyler B.; Ding, Tiping; Dunn, Philip J. H.; Gröning, Manfred; Holden, Norman E.; Meijer, Harro A. J. (2022-05-04). "Standard atomic weights of the elements 2021 (IUPAC Technical Report)". Pure and Applied Chemistry. doi:10.1515/pac-2019-0603. ISSN 1365-3075.
  3. ^ a b Zhang Y; Evans JRG; Zhang S (2011). "Corrected Values for Boiling Points and Enthalpies of Vaporization of Elements in Handbooks". J. Chem. Eng. Data. 56 (2): 328–337. doi:10.1021/je1011086.
  4. ^ "Gallium (CAS Number 7440-55-3) : Strem Product Catalog". Strem Chemicals Inc. Retrieved 4 December 2023.
  5. ^ a b c d Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
  6. ^ Ga(−3) has been observed in LaGa, see Dürr, Ines; Bauer, Britta; Röhr, Caroline (2011). "Lanthan-Triel/Tetrel-ide La(Al,Ga)x(Si,Ge)1-x. Experimentelle und theoretische Studien zur Stabilität intermetallischer 1:1-Phasen" (PDF). Z. Naturforsch. (in German). 66b: 1107–1121.
  7. ^ Hofmann, Patrick (1997). Colture. Ein Programm zur interaktiven Visualisierung von Festkörperstrukturen sowie Synthese, Struktur und Eigenschaften von binären und ternären Alkali- und Erdalkalimetallgalliden (PDF) (Thesis) (in German). PhD Thesis, ETH Zurich. p. 72. doi:10.3929/ethz-a-001859893. hdl:20.500.11850/143357. ISBN 978-3728125972.
  8. ^ Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN 0-8493-0464-4.
  9. ^ Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3): 030001. doi:10.1088/1674-1137/abddae.
  10. ^ W. L. Tsai, Y. Hwu, C. H. Chen, L. W. Chang, J. H. Je, H. M. Lin, G. Margaritondo (2003). "Grain boundary imaging, gallium diffusion and the fracture behavior of Al–Zn Alloy – An in situ study". Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms. 199: 457–463. doi:10.1016/S0168-583X(02)01533-1.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  11. ^ Vigilante, G. N., Trolano, E., Mossey, C. (Jun 1999). "Liquid Metal Embrittlement of ASTM A723 Gun Steel by Indium and Gallium". Defense Technical Information Center.{{cite web}}: CS1 maint: multiple names: authors list (link)
  12. ^ Sublette,Cary (2001-9-9). "Section 6.2.2.1". Nuclear Weapons FAQ. Retrieved 2008-01-24. {{cite web}}: Check date values in: |date= (help)
  13. ^ Mark Winter. "Scholar Edition: gallium: Biological information". The University of Sheffield and WebElements Ltd, UK.
  14. ^ Shan Xiao-quan, Wang Wen and Wen Bei (1992). "Determination of gallium in coal and coal fly ash by electrothermal atomic absorption spectrometry using slurry sampling and nickel chemical modification". J. Anal. At. Spectrom. 7: 761–764. doi:10.1039/JA9920700761.
  15. ^ "Gallium in West Virginia Coals". West Virginia Geological and Economic Survey. 2 Mar 2002.
  16. ^ O. Font, X. Querol, R. Juan, R. Casado, C. R. Ruiz, A. Lopez-Soler, P. Coca and F. G. Pena (2007). "Recovery of gallium and vanadium from gasification fly ash". Journal of Hazardous Materials. 139 (3): 413–423. doi:10.1016/j.jhazmat.2006.02.041.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  17. ^ A. J. W. Headlee and Richard G. Hunter (1953). "Elements in Coal Ash and Their Industrial Significance". Industrial and Engineering Chemistry. 45 (3): 548–551. doi:10.1021/ie50519a028.
  18. ^ Augsberg University Calculate When Our Materials Run Out retrieved May 4, 2008
  19. ^ "Purdue Energy Center symposium to pave the road to a hydrogen economy" (Press release). Purdue University. April 10, 2007.
  20. ^ "New process generates hydrogen from aluminum alloy to run engines, fuel cells". PhysOrg.com. 16 May 2007.
  21. ^ G. Eby (2005). "Elimination of arthritis pain and inflammation for over 2 years with a single 90 min, topical 14% gallium nitrate treatment: Case reports and review of actions of gallium III". Medical Hypotheses. 65 (6): 1136–1141. doi:10.1016/j.mehy.2005.06.021.
  22. ^ L. R. Bernstein, T. Tanner, C. Godfrey, B. Noll (2000). "Chemistry and pharmacokinetics of gallium maltolate, a compound with high oral gallium bioavailability". Metal Based Drugs. 7: 33–48. doi:10.1155/MBD.2000.33.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
  23. ^ A Trojan-horse strategy selected to fight bacteria
  24. ^ Gallium May Have Antibiotic-Like Properties


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