Emanations from Actinium.
146. Debierne[[240]] found that actinium gives out an emanation similar to the emanation of thorium and radium. The loss of activity of the emanation is even more rapid than for the thorium emanation, for its activity falls to half value in 3·9 seconds. In consequence of the rapid decay of activity, the emanation is able to diffuse through the air only a short distance from the active matter before it loses the greater proportion of its activity. Giesel early observed that the radio-active substance separated by him, which we have seen ([section 18]) is identical in radio-active properties with actinium, gave off a large amount of emanation. It was in consequence of this property, that he gave it the name of the “emanating substance” and later “emanium.” The impure preparations of this substance emit the emanation very freely and in this respect differ from most of the thorium compounds. The emanation from actinium like those from thorium and radium possesses the property of exciting activity on inactive bodies, but it has not yet been studied so completely as the better known emanations of thorium and radium.
Experiments with large amounts of Radium Emanation.
147. With very active specimens of radium a large amount of emanation can be obtained, and the electrical, photographic, and fluorescent effects are correspondingly intense. On account of the small activity of thorium and the rapid decay of its emanation the effects due to it are weak, and can be studied only for a few minutes after its production. The emanation from radium, on the other hand, in consequence of the slow decay of its activity, may be stored mixed with air in an ordinary gas-holder, and its photographic and electrical actions may be examined several days or even weeks after, quite apart from those of the radium from which it was obtained.
It is, in general, difficult to study the radiation due to the emanation alone, on account of the fact that the emanation is continually producing a secondary type of activity on the surface of the vessel in which the emanation is enclosed. This excited activity reaches a maximum value several hours after the introduction of the emanation, and, as long as it is kept in the vessel, this excited activity on the walls decays at the same rate as the emanation itself, i.e. it falls to half its initial value in about 4 days. If, however, the emanation is blown out, the excited activity remains behind on the surface, but rapidly loses its activity in the course of a few hours. After several hours the intensity of the residual radiation is very small.
These effects and their connection with the emanation are discussed more fully in [chapter VIII]. Giesel[[241]] has recorded some interesting observations of the effect of the radium emanation on a screen of phosphorescent zinc sulphide. When a few centigrams of moist radium bromide were placed on a screen any slight motion of the air caused the luminosity to move to and fro on the screen. The direction of phosphorescence could be altered at will by a slow current of air. The effect was still further increased by placing the active material in a tube and blowing the air through it towards the screen. A screen of barium platinocyanide or of Balmain’s paint failed to give any visible light under the same conditions. The luminosity was not altered by a magnetic field, but it was affected by an electric field. If the screen were charged the luminosity was more marked when it was negative than when it was positive.
Giesel states that the luminosity was not equally distributed, but was concentrated in a peculiar ring-shaped manner over the surface of the screen. The concentration of luminosity on the negative, rather than on the positive, electrode is probably due to the excited activity, caused by the emanation, and not to the emanation itself, for this excited activity is concentrated chiefly on the negative electrode in an electric field (see [chapter VIII]).
An experiment to illustrate the phosphorescence produced in some substances by the rays from a large amount of emanation is described in [section 165].
148. Curie and Debierne[[242]] have investigated the emanation from radium, and the excited activity produced by it. Some experiments were made on the amount of emanation given off from radium under very low pressures. The tube containing the emanation was exhausted to a good vacuum by a mercury pump. It was observed that a gas was given off from the radium which produced excited activity on the glass walls. This gas was extremely active, and rapidly affected a photographic plate through the glass. It caused fluorescence on the surface of the glass and rapidly blackened it, and was still active after standing ten days. When spectroscopically examined, this gas did not show any new lines, but generally those of the spectra of carbonic acid, hydrogen, and mercury. In the light of the results described in [section 124] the gas, given off by the radium, was probably the non-active gases hydrogen and oxygen, in which the active emanation was mixed in minute quantity. It will be shown later ([section 242]) that the energy radiated from the emanation is enormous compared with the amount of matter involved, and that the effects observed, in most cases, are produced by an almost infinitesimal amount of the emanation.
In further experiments, Curie and Debierne[[243]] found that many substances were phosphorescent under the action of the emanation and the excited activity produced by it. In their experiments, two glass bulbs A and B ([Fig. 54]) were connected with a glass tube. The active material was placed in the bulb A and the substance to be examined in the other.