Properties | More Info | Isotopes | Spectra
Compounds | Reactions | Production
Atomic: M.A.C. | Reference
Diagrams: Shell | Atomic Radius | Electron || Images
Praseodymium [Pr] locate me
CAS-ID: 7440-10-0
An: 59 N: 82
Am: 140.90765(2) g/mol
Group Name: Lanthanoids
Block: f-block  Period: 6 (lanthanoid)
State: solid at 298 K
Colour: silvery white, yellowish tinge Classification: Metallic
Boiling Point: 3563K (3290°C)
Melting Point: 1208K (935°C)
Density: 6.77g/cm3
Discovery Information
Who: C.F. Aver von Welsbach
When: 1885
Where: Austria
Name Origin
Greek: prasios (green) and didymos (twin); from its green salts.
 "Praseodymium" in different languages.
Sources
Can be found in rare earth minerals such as bastnasite and monazite. Obtained from the same salts as neodymium.
Primary producers are the USA, Brazil, India, Sri Lanka and Australia. Annual production is around 2400 tons.
Abundance
 Universe: 0.002 ppm (by weight)
 Sun: 0.001 ppm (by weight)
 Carbonaceous meteorite: 0.1 ppm
 Earth's Crust: 8.7 ppm
 Seawater:
   Atlantic surface: 4 x 10-7 ppm
   Atlantic deep: 7 x 10-7 ppm
   Pacific surface: 4.4 x 10-7 ppm
   Pacific deep: 1 x 10-6 ppm
Uses
Praseodymium forms the core of carbon arc lights which are used in the motion picture industry for studio lighting and projector lights.
Used for colouring glass and ceramic glazes. Also used with neodymium to make lenses for glass maker's goggles because they filter out the yellow light present in glass blowing. It is alloyed with magnesium to create high strength metals.
History
In 1841, Mosander extracted the rare earth didymium from lanthana. In 1874, Per Teodor Cleve concluded that didymium was in fact two elements, and in 1879, Lecoq de Boisbaudran isolated a new earth, samarium, from didymium obtained from the mineral samarskite. In 1885, the Austrian chemist baron Carl Auer von Welsbach separated didymium into two elements, praseodymium and neodymium, which gave salts of different colours.
Leo Moser investigated the use of praseodymium in glass colouration in the late 1920s. The result was a yellow-green glass given the name "Prasemit". However, a similar colour could be achieved with colourants costing only a minute fraction of what praseodymium cost in the late 1920s, such that the colour was not popular, few pieces were made, and examples are now extremely rare. Moser also blended praseodymium with neodymium to produce "Heliolite" glass ("Heliolit" in German), which was more widely accepted. The first enduring commercial use of praseodymium, which continues today, is in the form of a yellow-orange stain for ceramics, "Praseodymium Yellow", which is a solid-solution of praseodymium in the zirconium silicate (zircon) lattice. This stain has no hint of green in it. By contrast, at sufficiently high loadings, praseodymium glass is distinctly green, rather than pure yellow.
Praseodymium has historically been a rare earth whose supply has exceeded demand. Unwanted as such, much praseodymium has been marketed as a mixture with lanthanum and cerium, or "LCP" for the first letters of each of the constituents, for use in replacing the traditional lanthanoid mixtures that were inexpensively made from monazite or bastnaesite. LCP is what remains of such mixtures, after the desirable neodymium, and all the heavier, rarer and more valuable lanthanoids have been removed, by solvent extraction. However, as technology progresses, praseodymium has been found possible to incorporate into neodymium-iron-boron magnets, thereby extending the supply of the much in demand neodymium. So LC is starting to replace LCP as a result.
Notes
Dr. Matthew Sellars of the Laser Physics Centre at the Australian National University in Canberra, Australia slowed down a light pulse to a few hundred meters per second using Praseodymium mixed with silicate crystal.
Hazards
Like all rare earth elements, praseodymium is of low to moderate toxicity. Praseodymium has no known biological role.