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This is not to say that specialists should confine 'l'.he earlier methods of reduction of the magnesia
themselves entirely to their own subjects. Both by an alkali metal have now only historical inte~est,
parties must know the groundwork of the other but in 1830 Faraday decomposed molten magnesi?ID
subject for a collaboration to be successful. The chloride electrolytically; and in 1852, Bunsen im-
specialization on insecticides research should resemble proved this process and thus laid the foundation of
mountain peaks connected by ridges and passes, and that most widely used to-day. There are great
not the isolated specialization of the branches of a advantages in employing a proc~ss which yields ~he
tree. That is probably true for other types of research anliydrous chloride in one operation; the alternative
also. is to expel water from the hydrated salt, the last
two molecules of water in which are retained some-
1
Tattersfleld, F., Ann. Appl. Biol., 26, 865 (1989).
• Cotton, R. T., J. Ecmi. Emom:, 25, 1088 (1982). what firmly, the dehydration then often r~ulting
• Tattersfleld , F., and others, J. Agric. Sci., 10, 199 (1920); 17, 181 the formation of the oxide and oxychlor1de. ThlS
(1927). may be effected by taking advantage of the reaction
• Tattersfleld, F., and others, Ann. Appl. Biol., 12, 218 (1925); 13, between magnesia, dry chlorine and carbon.
' 424 (1926).
• Ferguson, J., Proc. R<l/1. Soc;, B, 127, 887 (1989). MgO+C+Cl,--+ MgCl,+CO,
'Busvine, J. R., NATURE, 150, 208 (1942). 2Mgo+c+2c1.--+ 2Mg01.+co,.
' Hazelhoff, E. H., Z. vergl. PhY8iol., Ii, 179 (1927).
• Wigglesworth, V. B., Bu/I. Em. Re8., 33, 205 (1942). As both these reactions are exothermic, the heat
• Krilger, F., Z. d. angew. Entom., 18, 344 (1931), and others. required is not great. The ground magnesia ~s mixed
'.' Hurst, H., NATURE, 145, 462 (1940). with carbon in the form of coke or anthracite dust,
"Clark, A. J., "The Mode of Action of Drugs on Cells" (London:
Arnold and Co., 1935). together with some material, such as sawdust or peat,
to make the mass porous, and made into briquettes.
Molten magnesium clµoride in the anhydrous state
is then tapped off from t~e base of t~e furna~e.
Theoretically, the chlorme process 1s a cyclic one,
PRODUCTION OF MAGNESIUM the c4lorine absorbed in the chlorination plant being
again set free in the electrolytic cell. In practice,
M AGNESIUM is to-day a me~l of the_great~st
importance, and the paucity of reliable m-
forma.tion regarding the production of this la.test
however this recovery is by no means complete, a
fa.ct whi~h is partly due to the formation of hydro-
chloric acid with moisture. It is necessary, there-
addition to the industrially important metals makes fore, both to add chlorine from some other sou~ce
especially welcome the survey given by Dr. C. H. and ·to absorb the acid fumes in some sort of washmg
Desch in the Peter Le Neve Foster Lecture to the plant.
Royal Society of Arts delivered on February 17. Full details of the electrolytic practice are not
Magnesium, the lightest of all the industrial metals, generally available, but in broad outline this consists
is a new-comer to metallurgy. Although first pre- of rectangular steel cells with graphite anodes and
pared by Davy in 1808, it has only become really iron cathodes. The bath of fosed salts usually con-
well known in the course of ·the present W a.r, though tains chlorides of the alkali or alkali-earth metals
its production had been increasing for some years in addition to the magnesium chloride, in order to
before.
lower the melting point as well as to lessen the deco~-
The pure carbonate is of only local occurrence, position, which is appreciable w~en the pure salt 1s
though there are very large deposits of a lower degree kept in the molten state. Fluorides are also some-
of purity. The double carbonate of calcium and times added. On account of the low density of mag-
magnesium, dolomite, is far more widely distributed, nesium it floats on the surface, rendering it necessary
and sea water provides an inexhaustible source of to pro~ide for the complete separation of the upp~r
the chloride in a dilute form, while certain con- parts of the anode and cathode compartments, m
centrated solutions of magnesium salts occur in the order to prevent contact of the metal and t_he chlori~e
Dead Sea and elsewhere.
produced. The partitions a:re of ceramic material
The fact that magnesium alloys are available which immersed from above. Large electrodes of good de-
are extremely light for a given strength renders the sign are also necessary, each cell usually carrying
new metal one of great importance in all branches of 15-20 000 amp. with a potential difference of 7-9
transport engineering. The output of the United volts;' The bath temperature varies from 670° to
States is planned at a rate of some hundred times 750° C., the energy consumption being_ abo?t 2~ kWh.
that of 1940, but the industry is f~r from being merely per kgm. of metal. The liquid_ magnesium 1s s~mmed
a war-time one and will certainly play a permanent off from time to time, and with modern castmg and
part in both metallurgy and engineering. remelting technique a very pur,e met_a l is o~tained
The preparation of magnesia from sea water is not free from the inclusions of hygroscopic chlorides to
new, going back to the early days of the basic which corrosion was once attributed.
Bessemer process, but it is only in very recent years Attempts to manufacture magnes~um by pro?e~ses
that it has b~come of real importance. Oceanic similar to that used in the extraction of alummium
water contains about O•14 per cent of magnesium, and have so far proved a costly fi:~il~e in the Un~ted
the process is represented by the simple reaction : States. The solubility of magnesia m molten fluorides
MgCl1 + Ca(OH). -+ Mg(OH) + CaCl 2 2,
is much less than that of alumina in cryolite, and the
salt baths have both a higher melting point and
the relatively insoluble magnesium hydroxide being density. . ..
precipitated. It is, however, often necessary to re- Magnesium being a volatil~ metal boilmg :1t
move other salts by the addition of lime prior to the 1097° C. the reduction of the oxide by a non-volatile
recovery of the magnesium, and conditions must be reducing agent, carbon, calcium carbide, ·rerro-
so adjusted that the particles are of such a size as to silicon aluminium, etc., and the removal of the metal
filter rapidly. By using calcined dolomite instead in the' form of vapour has suggested itself to sevt:ral
of lime, the yield is increased. inventors. The presence of even a small proport10n