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CHAPTER VI. CONTINUOUS PRODUCTION OF RADIO-ACTIVE MATTER.

constant activity of the radio-elements is due to an equilibrium process, in which the rate of production of fresh active matter balances the rate of change of that already formed.

The nature of the process taking place in the radio-elements, in order to give rise to the production at a constant rate of new kinds of active matter, will now be considered. Since in thorium or uranium compounds there is a continuous production of radio-active matter, which differs in chemical properties from the parent substance, some kind of change must be taking place in the radio-element. This change, by which new matter is produced, is very different in character from the molecular changes dealt with in chemistry, for no chemical change is known which proceeds at the same rate at the temperatures corresponding to a red heat and to liquid air, and is independent of all physical and chemical actions. If, however, the production of active matter is supposed to be the result of changes, not in the molecule, but in the atom itself, it is not to be expected that the temperature would exert much influence. The general experience of chemistry in failing to transform the elements by the action of temperature is itself strong evidence that wide ranges of temperature have not much effect in altering the stability of the chemical atom.

The view that the atoms of the radio-elements are undergoing spontaneous disintegration was put forward by Rutherford and Soddy as a result of evidence of this character. The discovery of the material nature of the α rays added strong confirmation to the hypothesis; for it has been pointed out (section 95) that the expulsion of α particles must be the result of a disintegration of the atoms of the radio-element. Taking the case of thorium as an example, the processes occurring in the atom may be pictured in the following way. It must be supposed that the thorium atoms are not permanently stable systems, but, on an average, a constant small proportion of them—about one atom in every 1016 will suffice—break up per second. The disintegration consists in the expulsion from the atom of one or more α particles with great velocity. For simplicity, it will be supposed that each atom expels one α particle. It has been shown that the α particle of radium has a mass about twice that of the hydrogen atom. From the similarity of the α rays from thorium and radium, it is probable that the α particle of thorium does not differ much in mass from that of radium, and may be equal to it. The α particles expelled from the thorium atoms as they break up constitute what is known as the “non-separable activity” of thorium. This activity, measured by the α rays, is about 25 per cent. of the maximum. After the escape of an α particle, the part of the atom left behind, which has a mass slightly less than that of the thorium atom, tends to rearrange its components to form a temporarily stable system. It is to be expected that it will differ in chemical properties from the thorium atom from which it was derived. The atom of the substance Th X is, on this view, the thorium atom minus one α particle. The atoms of Th X are far more unstable than the atoms of thorium, and one after the other they break up, each atom expelling one α particle as before. These projected α particles give rise to the radiation from the Th X. Since the activity of Th X falls to half its original value in about four days, on an average half of the atoms of Th X break up in four days, the number breaking up per second being always proportional to the number present. After an atom of Th X has expelled an α particle, the mass of the system is again reduced, and its chemical properties are changed. It will be shown (section 154) that the Th X produces the thorium emanation, which exists as a radio-active gas, and that this in turn is transformed into matter which is deposited on solid bodies and gives rise to the phenomena of excited activity. The first few successive changes occurring in thorium are shown diagrammatically below (Fig. 50).

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