CHAPTER VIII
RADIOACTIVITY OF THE MINERALS

In the present chapter no attempt will be made to give a complete account of all the phenomena of radioactivity which have been observed in the mineral world. There are, however, a few problems of the highest scientific interest which centre about the rare earth minerals, and mention of these can hardly be avoided in a work which professes to give a general account of the rare earth group. It is obvious that a detailed treatment cannot be given without entering into phenomena which would be quite beyond the range of the present work, and an excuse is hardly needed, therefore, for the fragmentary and abbreviated account which follows. The reader’s acquaintance with the general phenomena of radioactivity is of necessity assumed.

Radioactivity (the spontaneous emission of special radiations) was first observed by Becquerel, in 1896, in the case of potassium uranyl sulphate, and was soon found to be common to all uranium compounds, and to the metal itself. Mme. Curie showed that whilst in uranium salts the degree of activity varies directly with the percentage of uranium, in minerals containing the element the same rule does not hold. The observation that pitchblende is considerably more active than the uranium it contains led to the discovery of polonium[125] and radium in 1898. Exactly analogous phenomena were shown to hold for thorium salts and thorium-containing minerals by Mme. Curie and Schmidt in 1898, and in 1905 Hahn separated Radio-thorium from thorianite. In 1899 Debierne discovered that the rare earths precipitated from the solution obtained on treatment of pitchblende are associated with another extremely active body, which he named Actinium; Giesel found that in the separation of the rare earths this remains with lanthanum. In 1903 Ramsay and Soddy experimentally confirmed the prediction of Rutherford and Soddy, that radium would be found to produce helium continuously. The discovery of these remarkable phenomena has modified many fundamental physical conceptions, and has opened up a new field of scientific enquiry, which is being developed with unexampled rapidity.

[125] Polonium, which was named by Mme. Curie in honour of her native country, has been shown to be identical with Marckwald’s ‘Radio-tellurium,’ which was named by Rutherford ‘Radium F’; it is one of the degradation products of radium.

It has been mentioned, in the accounts of the rare earth minerals given above, that almost all these minerals are radioactive, i.e. have the property of emitting specific radiations. Moreover, radioactivity, to any considerable extent at least, is, with a few important exceptions, confined to the minerals which have been already described. It has been shown by many investigators, chief amongst whom are Strutt and Boltwood, that the activity is usually due to the presence of uranium or thorium, or both.[126]

[126] Hauser and Wirth (Ber. 1910, 43, 1807) observed activity in some zirconium minerals containing neither thorium nor uranium.

After the discovery of helium in Cleveite (a variety of pitchblende, vide [p. 13]) in 1895 by Ramsay, a large number of minerals were examined for this gas, and it was found that almost all the rare earth minerals contain helium. The fact that these minerals are also for the most part radioactive, naturally suggested some relation between the activity and the presence of helium, and led directly to the discovery that radium is continuously producing helium; and it became apparent that helium has been accumulating in these minerals since their formation, by the decay of radioactive elements. The question of the origin of helium in minerals will be touched on [again].

In 1904 Boltwood advanced the theory that radium is produced by the degradation of uranium, the parent-element having, however, a much greater half-life period. If uranium continuously produces radium, whilst the latter decays much more rapidly than the former, it must follow that in minerals containing uranium a state of equilibrium is reached between uranium and radium, and the ratio of these two in all minerals should therefore be constant, and independent of the geological age. Boltwood examined a number of the minerals of which descriptions have been given in the preceding chapters, and found the ratio to be surprisingly constant.[127] Strutt also examined a large number of minerals,[128] and whilst on the whole his results seemed to support the theory, his values for the ratio were by no means so constant as those of Boltwood. Strutt included in his examination the interesting radium-containing mineral observed by Danne at Issy l’Evêque.[129] This was a pyromorphite (lead chlorophosphate) containing neither uranium nor thorium. Danne suggested that the radium was not an original constituent, but had been introduced by the action of percolating waters. This view was confirmed by McCoy and Ross,[130] who found that the activity was entirely confined to the surface layer.

[127] Amer. J. Sci. 1904, [iv.], 18, 97; Phil. Mag. 1905, [iv.], 9, 599.

[128] Proc. Roy. Soc. 1905, A, 76, 88 and 312. Ibid. 1907, A, 80, 56.