Praseodymium

Praseodymium, 59Pr
Praseodymium
Pronunciation/ˌpreɪziːəˈdɪmiəm/ (listenⓘ) ​(PRAY-zee-ə-DIM-ee-əm)
Appearancegrayish white
Standard atomic weight Ar°(Pr)
140.90766(1)
Praseodymium 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
–
↑
Pr
↓
Pa
cerium ← praseodymium → neodymium
Atomic number (Z)59
Groupf-block groups (no number)
Periodperiod 6
Block  f-block
Electron configuration[Xe] 4f3 6s2
Electrons per shell2, 8, 18, 21, 8, 2
Physical properties
Phase at STPsolid
Melting point1208 K ​(935 °C, ​1715 °F)
Boiling point3403 K ​(3130 °C, ​5666 °F)
Density (near r.t.)6.77 g/cm3
when liquid (at m.p.)6.50 g/cm3
Heat of fusion6.89 kJ/mol
Heat of vaporization331 kJ/mol
Molar heat capacity27.20 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1771 1973 (2227) (2571) (3054) (3779)
Atomic properties
Oxidation states0, +1, +2, +3, +4, +5 (a mildly basic oxide)
ElectronegativityPauling scale: 1.13
Ionization energies
  • 1st: 527 kJ/mol
  • 2nd: 1020 kJ/mol
  • 3rd: 2086 kJ/mol
Atomic radiusempirical: 182 pm
Covalent radius203±7 pm
Color lines in a spectral range
Spectral lines of praseodymium
Other properties
Natural occurrenceprimordial
Crystal structure ​double hexagonal close-packed (dhcp)
Double hexagonal close packed crystal structure for praseodymium
Speed of sound thin rod2280 m/s (at 20 °C)
Thermal expansionα, poly: 6.7 µm/(m⋅K) (at r.t.)
Thermal conductivity12.5 W/(m⋅K)
Electrical resistivityα, poly: 0.700 µΩ⋅m (at r.t.)
Magnetic orderingparamagnetic
Molar magnetic susceptibility+5010.0×10−6 cm3/mol (293 K)
Young's modulusα form: 37.3 GPa
Shear modulusα form: 14.8 GPa
Bulk modulusα form: 28.8 GPa
Poisson ratioα form: 0.281
Vickers hardness250–745 MPa
Brinell hardness250–640 MPa
CAS Number7440-10-0
History
DiscoveryCarl Auer von Welsbach (1885)
Isotopes of praseodymium
Main isotopes Decay
abun­dance half-life (t1/2) mode pro­duct
141Pr 100% stable
142Pr synth 19.12 h β− 142Nd
ε 142Ce
143Pr synth 13.57 d β− 143Nd
 Category: Praseodymium
| references
Praseodymium

Praseodymium is a chemical element that has the symbol Pr on the periodic table. It has the atomic number 59 which means it has 59 protons in an atom. It is a soft silvery metal that can be used to make yellow-green salts. It is mixed with magnesium to produce strong metal used in aircraft engines. It can also be used to color green glass, and is in electrodes in lights. Praseodymium was first isolated (separated from other elements) in 1885 by the Austrian chemist Carl Auer von Welsbach. It is found in sands, called monazite sands, of Florida, California, India, and Brazil.

Estimates of Praseodymium that can be mined

"Praseodymium [can be found in, or is] a companion in the ... minerals Cerit, Monazit and Bastnäsit. The worldwide reserves are estimated at 4 million tons", according to media (in 2024's second quarter).

Sources

  1. ↑ "praseodymium". Oxford English Dictionary. Oxford University Press. 2nd ed. 1989.
  2. ↑ "Standard Atomic Weights: Praseodymium". CIAAW. 2017.
  3. ↑ 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.
  4. ↑ Chen, Xin; et al. (2019-12-13). "Lanthanides with Unusually Low Oxidation States in the PrB3– and PrB4– Boride Clusters". Inorganic Chemistry. 58 (1): 411–418. doi:10.1021/acs.inorgchem.8b02572. PMID 30543295. S2CID 56148031.
  5. ↑ Jackson, M. (2000). "Magnetism of Rare Earth" (PDF). The IRM quarterly. 10 (3): 1.
  6. ↑ Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN 0-8493-0464-4.
  7. ↑ 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.
  8. ↑ https://investingnews.com/daily/resource-investing/critical-metals-investing/rare-earth-investing/rare-earth-reserves-country/. Retrieved 2024-06-08