Terbium

Terbium, 65Tb
Terbium
Pronunciation/ˈtɜːrbiəm/ (TUR-bee-əm)
Appearancesilvery white
Standard atomic weight Ar°(Tb)
Terbium 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


Tb

Bk
gadoliniumterbiumdysprosium
Atomic number (Z)65
Groupf-block groups (no number)
Periodperiod 6
Block  f-block
Electron configuration[Xe] 4f9 6s2
Electrons per shell2, 8, 18, 27, 8, 2
Physical properties
Phase at STPsolid
Melting point1629 K ​(1356 °C, ​2473 °F)
Boiling point3396 K ​(3123 °C, ​5653 °F)
Density (at 20° C)8.229 g/cm3[3]
when liquid (at m.p.)7.65 g/cm3
Heat of fusion10.15 kJ/mol
Heat of vaporization391 kJ/mol
Molar heat capacity28.91 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1789 1979 (2201) (2505) (2913) (3491)
Atomic properties
Oxidation statescommon: +3
0,[4] +1,[5] +2,[6] +4[7]
ElectronegativityPauling scale: 1.2 (?)
Ionization energies
  • 1st: 565.8 kJ/mol
  • 2nd: 1110 kJ/mol
  • 3rd: 2114 kJ/mol
Atomic radiusempirical: 177 pm
Covalent radius194±5 pm
Color lines in a spectral range
Spectral lines of terbium
Other properties
Natural occurrenceprimordial
Crystal structurehexagonal close-packed (hcp) (hP2)
Lattice constants
Hexagonal close packed crystal structure for terbium
a = 360.56 pm
c = 569.66 pm (at 20 °C)[3]
Thermal expansionat r.t. poly: 10.3 µm/(m⋅K)
Thermal conductivity11.1 W/(m⋅K)
Electrical resistivityα, poly: 1.150 µΩ⋅m (at r.t.)
Magnetic orderingparamagnetic at 300 K
Molar magnetic susceptibility+146000×10−6 cm3/mol (273 K)[8]
Young's modulus55.7 GPa
Shear modulus22.1 GPa
Bulk modulus38.7 GPa
Speed of sound thin rod2620 m/s (at 20 °C)
Poisson ratio0.261
Vickers hardness450–865 MPa
Brinell hardness675–1200 MPa
CAS Number7440-27-9
History
Namingafter Ytterby (Sweden), where it was mined
Discovery and first isolationCarl Gustaf Mosander (1843)
Isotopes of terbium
Main isotopes[9] Decay
abun­dance half-life (t1/2) mode pro­duct
157Tb synth 71 y ε 157Gd
158Tb synth 180 y ε 158Gd
β 158Dy
159Tb 100% stable
 Category: Terbium
| references

Terbium is a chemical element; it has the symbol Tb and atomic number 65. It is a silvery-white, rare earth metal that is malleable and ductile. The ninth member of the lanthanide series, terbium is a fairly electropositive metal that reacts with water, evolving hydrogen gas. Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite, xenotime and euxenite.

Swedish chemist Carl Gustaf Mosander discovered terbium as a chemical element in 1843. He detected it as an impurity in yttrium oxide (Y2O3). Yttrium and terbium, as well as erbium and ytterbium, are named after the village of Ytterby in Sweden. Terbium was not isolated in pure form until the advent of ion exchange techniques.

Terbium is used to dope calcium fluoride, calcium tungstate and strontium molybdate in solid-state devices, and as a crystal stabilizer of fuel cells that operate at elevated temperatures. As a component of Terfenol-D (an alloy that expands and contracts when exposed to magnetic fields more than any other alloy), terbium is of use in actuators, in naval sonar systems and in sensors. Terbium is considered non-hazardous, though its biological role and toxicity has not been researched in depth.

Most of the world's terbium supply is used in green phosphors. Terbium oxide is used in fluorescent lamps and television and monitor cathode-ray tubes (CRTs). Terbium green phosphors are combined with divalent europium blue phosphors and trivalent europium red phosphors to provide trichromatic lighting technology, a high-efficiency white light used in indoor lighting.

  1. ^ "Standard Atomic Weights: Terbium". CIAAW. 2021.
  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 Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
  4. ^ Yttrium and all lanthanides except Ce and Pm have been observed in the oxidation state 0 in bis(1,3,5-tri-t-butylbenzene) complexes, see Cloke, F. Geoffrey N. (1993). "Zero Oxidation State Compounds of Scandium, Yttrium, and the Lanthanides". Chem. Soc. Rev. 22: 17–24. doi:10.1039/CS9932200017. and Arnold, Polly L.; Petrukhina, Marina A.; Bochenkov, Vladimir E.; Shabatina, Tatyana I.; Zagorskii, Vyacheslav V.; Cloke (2003-12-15). "Arene complexation of Sm, Eu, Tm and Yb atoms: a variable temperature spectroscopic investigation". Journal of Organometallic Chemistry. 688 (1–2): 49–55. doi:10.1016/j.jorganchem.2003.08.028.
  5. ^ La(I), Pr(I), Tb(I), Tm(I), and Yb(I) have been observed in MB8 clusters; see Li, Wan-Lu; Chen, Teng-Teng; Chen, Wei-Jia; Li, Jun; Wang, Lai-Sheng (2021). "Monovalent lanthanide(I) in borozene complexes". Nature Communications. 12 (1): 6467. doi:10.1038/s41467-021-26785-9. PMC 8578558. PMID 34753931.
  6. ^ All the lanthanides, except Pm, in the +2 oxidation state have been observed in organometallic molecular complexes, see Lanthanides Topple Assumptions and Meyer, G. (2014). "All the Lanthanides Do It and Even Uranium Does Oxidation State +2". Angewandte Chemie International Edition. 53 (14): 3550–51. doi:10.1002/anie.201311325. PMID 24616202.. Additionally, all the lanthanides (La–Lu) form dihydrides (LnH2), dicarbides (LnC2), monosulfides (LnS), monoselenides (LnSe), and monotellurides (LnTe), but for most elements these compounds have Ln3+ ions with electrons delocalized into conduction bands, e. g. Ln3+(H)2(e).
  7. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 28. ISBN 978-0-08-037941-8.
  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.