The Rare Earths: Their Occurrence, Chemistry, and TechnologyLevy, Stanley Isaac
Science
The Rare Earths: Their Occurrence, Chemistry, and Technology
Levy, Stanley Isaac
Rare earths
3863·52
3951·32
4061·27
4156·30
4247·54
4282·67
4303·78
4325·87
4375·11
4385·81
4400·96
4446·51
4451·71
4463·09
4920·84
5923·35
5319·98
5594·58
5620·75
6310·69
6314·69
6385·32
~Samarium~, Sa = 150·4
The samarium of the earlier chemists (see p. 168) contained a large
proportion of the terbium elements, from which a fairly complete
separation was first effected by Demarçay in 1900.[291] By the
fractional crystallisation of the double magnesium nitrate in presence
of bismuth magnesium nitrate, Urbain and Lacombe[292] succeeded in
preparing samarium compounds, which were shown by spectroscopic
examination[293] to be free from other earths. The element is
intermediate in electropositive character and in the solubility
relations of its salts between neodymium and the terbium earths; its
salts are topaz-yellow in colour, and in concentrated solutions show
absorption in the blue and violet regions. The oxide is almost white in
colour, with only a faint yellow tinge. A systematic investigation of
samarium compounds was carried out by Cleve,[294] but his work was
vitiated by the fact that his material was very impure. More recently,
the pure salts have been examined by Matignon and his pupils.
[291] _Compt. rend._ 1900, ~130~, 1185.
[292] _Ibid._ 1904, ~138~, 84 _and_ 1166.
[293] Eberhard, _Zeitsch. anorg. Chem._ 1905, ~45~, 374.
[294] _Trans. Chem. Soc._ 1883, ~43~, 362; _Bull. Soc. Chim._ 1885,
[ii.], ~43~, 53; _Chem. News_, 1886, ~53~, 30, 45, 67, 80, 91, 100.
The melting-point of the _metal_ lies between 1300° and 1400°C., so that
its preparation by the electrolytic method is a matter of great
difficulty. A mixture of the chloride with one-third of its weight of
barium chloride is electrolysed by means of a current of 100 ampères,
using a cathode of only 2·5 mm. thickness; the metal so obtained is
greyish white in colour, and is the hardest of the cerium elements.
The _chloride_ separates from aqueous solution as the hexahydrate,
SaCl₃,H₂O, in large tabular yellow crystals. The anhydrous chloride is
white, but fuses to a chocolate-brown liquid; it forms a large number of
additive compounds with ammonia. When heated in an atmosphere of dry
hydrogen or ammonia, air and moisture being carefully excluded, it
yields the _subchloride_,[295] SaCl₂, as a dark brown crystalline solid,
insoluble in alcohol and all organic solvents. Samarous chloride
dissolves in water, forming a deep brownish-red solution, which rapidly
becomes colourless, with evolution of hydrogen, and precipitation of the
oxide and oxychloride. _Samarous iodide_, SaI₂, may be obtained by a
similar process, and closely resembles the chloride.
[295] Matignon and Cazes, _Compt. rend._ 1906, ~142~, 83.
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