Bary[[185]] has made a very complete examination of the class of substances which become luminous under radium rays. He found that the great majority of substances belong to the alkali metals and alkaline earths. All these substances were also phosphorescent under the action of X rays.
Crystalline zinc sulphide (Sidot’s blende) phosphoresces very brightly under the influence of the rays from radium and other very active substances. This was observed by Curie and Debierne in their study of the radium emanation and the excited activity produced by it. It has also been largely used by Giesel as an optical means of detecting the presence of emanations from very active substances. It is an especially sensitive means of detecting the presence of α rays, when it exhibits the “scintillating” property already discussed in section 96. In order to show the luminosity due to the α rays, the screen should be held close to the active substance, as the rays are absorbed in their passage through a few centimetres of air. Zinc sulphide is also luminous under the action of the β rays, but the phosphorescence is far more persistent than when produced by the α rays.
Very beautiful luminous effects are produced by large crystals of the platinocyanides exposed to the radium rays. Those containing lithium give a brilliant pink colour. The calcium and barium salts fluoresce with a deep green light, and the sodium compound with a lemon yellow. The mineral willemite (zinc silicate) was recently found by Kunz to be an even more sensitive means of detecting the presence of the radiations than platinocyanide of barium. It fluoresces showing a beautiful greenish colour, and a piece of mineral exposed to the action of the rays appears quite translucent. The crystals of the platinocyanides of barium and lithium are especially suited for showing the action of the γ rays, and, in this respect, are superior to willemite.
A very striking effect is shown by the mineral kunzite—a new variety of spodumene discovered by Kunz[[186]]. This is a transparent gem like crystal, often of very large size, which glows with a beautiful reddish colour under the action of the β or γ rays, but does not appear to be sensitive to the α rays. The luminosity extends throughout the crystal, but is not so marked as in the platinocyanides or willemite. The mineral sparteite[[187]], a form of calcite containing a few per cent. of manganese, has been found by Ambrecht to fluoresce with a very deep orange light under the β and γ rays. The colour appears to depend on the intensity of the rays, and is deeper close to the radium than at some distance away.
If kunzite and sparteite are exposed to the action of the cathode rays in a vacuum tube, the colour is different from that produced by the radium rays. The former appears a deep yellow, instead of the deep red observed with the radium rays.
The different actions of the radium rays on these fluorescent substances can be illustrated very simply and beautifully by the following experiment. A small U tube is filled with fragments of the fluorescent substance arranged in layers. The U tube is immersed in liquid air and the emanation from about 30 mgrs. of radium bromide is condensed in the tube. On closing the tube and removing it from the liquid air, the emanation distributes itself uniformly in the tube. The shades of colour produced in the different substances are clearly seen.
It is observed that all the crystals increase in luminosity for several hours, on account of the excited activity produced by the emanation. This effect is especially observed in kunzite, which at first hardly responds to the rays, since the β and γ rays, which causes it to fluoresce, are not given out by the emanation itself but by one of its later products. The intensity of the β and γ rays is, in consequence, small at first but rises to a maximum after several hours; the luminosity observed varies in a corresponding manner.
Sir William Crookes[[188]] has made an examination of the effect of continued exposure of a diamond to the radium rays. An “off-colour” diamond, of a pale yellow colour, was placed inside a tube with radium bromide. After 78 days’ exposure, the diamond had darkened and become bluish green in tint; when heated at 50° in a mixture of potassium chlorate for ten days, the diamond lost its dull surface colour and was bright and transparent, and its tint had changed to a pale bluish green. The rays have thus a double action on the diamond; the less penetrating β rays produce a superficial darkening due to the change of the surface into graphite, while the more penetrating β rays and the γ rays produce a change of colour throughout its mass. The diamond phosphoresced brightly during the whole course of its exposure to the rays. Crookes also observed that the diamond still retained enough activity to affect a photographic plate 35 days after removal, although, during the period of 10 days, it was heated in a mixture sufficiently powerful to remove the outer skin of graphite. This residual activity may possibly be due to a slow transformation product of the emanation which is deposited on the surface of bodies (see [chapter XI]).
Marckwald observed that the α rays from radio-tellurium produced marked phosphorescence on some kinds of diamonds. An account of the various luminous effects produced on different gems by exposure to the radium and actinium rays has been given by Kunz and Baskerville[[189]].
Both zinc sulphide and platinocyanide of barium diminish in luminosity after exposure for some time to the action of the rays. To regenerate a screen of the latter, exposure to solar light is necessary. A similar phenomenon has been observed by Villard for a screen exposed to Röntgen rays. Giesel made a screen of platinocyanide of radio-active barium. The screen, very luminous at first, gradually turned brown in colour, and at the same time the crystals became dichroic. In this condition the luminosity was much less, although the active substance had increased in activity after preparation. Many of the substances which are luminous under the rays from active substances lose this property to a large extent at low temperatures[[190]].