Miss Brooks observed that the activity was not concentrated on the negative electrode in an electric field but was diffused uniformly over the walls of the vessel. This observation is of importance in considering the explanation of the anomalous effects exhibited by the active deposit of radium, which will be discussed in the following section.

228. Effect of the first rapid change. We have seen that the law of decay of activity, measured by the β or γ rays, can be explained very satisfactorily if the first 3-minute change is disregarded. The full theoretical examination of the question given in sections [197] and [198] and the curves of Figs. [72] and [73] show, however, that the presence of the first change should exercise an effect of sufficient magnitude to be detected in measurements of the activity due to the succeeding changes. The question is of great interest, for it involves the important theoretical point whether the substances A and B are produced independently of one another, or whether A is the parent of B. In the latter case, the matter A which is present changes into B, and, in consequence, the amount of B present after A is transformed should be somewhat greater than if B were produced independently. Since the change of A is fairly rapid, the effect should be most marked in the early part of the curve.

In order to examine this point experimentally, the curve of rise of activity, measured by the β rays, was determined immediately after the introduction of a large quantity of the radium emanation into a closed vessel. The curve of decay of activity on a body for a long exposure after removal of the emanation, and the rise of activity after the introduction of the emanation, are in all cases complementary to one another. While, however, it is difficult to measure with certainty whether the activity has fallen in a given time, for example, from 100 to 99 or 98·5, it is easy to be sure whether the corresponding rise of activity in the converse experiment is 1 or 1·5 per cent. of the final amount. [Fig. 92], curve I, shows the rise of activity (measured by the β rays) obtained for an interval of 20 minutes after the introduction of the emanation. The ordinates represent the percentage amount of the final activity regained at any time.

Curve III shows the theoretical curve obtained on the assumption that A is a parent of B. This curve is calculated from equation (9) discussed in [section 198], and λ1, λ2, λ3 are the values previously found.

Curve II gives the theoretical activity at any time on the assumption that the substances A and B arise independently. This is calculated from an equation of the same form as (8), [section 198].

Fig. 92.

It is seen that the experimental results agree best with the view that A and B arise independently. Such a conclusion, however, is of too great importance to be accepted before examining closely whether the theoretical conditions are fulfilled in the experiments. In the first place, it is assumed that the carriers which give rise to excited activity are deposited on the surface of the body, to be made active immediately after their formation. There is some evidence, however, that some of these carriers exist for a considerable interval in the gas before their deposit on the body. For example, it is found that if a body is introduced for a short interval, about 1 minute, into a vessel containing the radium emanation, which has remained undisturbed for several hours, the activity after the first rapid decay (see [Fig. 86], curve B) is in much greater proportion than if an electric field had been acting for some time previously. This result indicates that the carriers of B and C both collect in the gas and are swept to the electrode when an electric field is applied. I have also observed that if radium emanation, which has stood undisturbed for some time, is swept into a testing vessel, the rise curve is not complementary to the decay curve, but indicates that a large amount of radium B and C was present with the emanation. The experiments of Miss Brooks, previously referred to, indicate that radium B does not obtain a charge and so will remain in the gas. Dr. Bronson, working in the laboratory of the writer, has obtained evidence that a large amount of radium D remains in the gas even in a strong electric field. If the matter B exists to some extent in the gas, the difference between the theoretical curves for three successive changes would be explained; for, in transferring the emanation to another vessel, the matter B mixed with it would commence at once to change into C and give rise to a part of the radiation observed.

The equal division of the activity between the products A and C (see [Fig. 90]) supports the view that C is a product of A, for when radio-active equilibrium is reached, the number of particles of A changing per second is equal to the number of B or C changing per second. If each atom of A and C expels an α particle of the same mass and with the same average velocity, the activity due to the matter A should be equal to that due to the matter C; and this, as we have seen, is the case.

While it is a matter of great difficulty to give a definite experimental proof that radium A and B are consecutive products, I think there is little doubt of its correctness. Accurate determinations of the curves of rise and decay may throw further light on the complicated processes which undoubtedly occur between the breaking up of the atoms of the emanation and the appearance of the active deposit on the electrodes.