The electric field required to produce practical saturation varies with
the intensity of the ionization and consequently with the activity of
the preparations to be examined. For preparations which have an activity
not more than 500 times that of uranium, under ordinary conditions, a
field of 100 volts per cm. is sufficient to produce a practical
saturation current. For very active samples of radium, it is often
impossible to obtain conveniently a high enough electromotive force to
give even approximate saturation. Under such conditions comparative
measurement can be made by measuring the current under diminished
pressure of the gas, when saturation is more readily obtained.
The method to be employed in the measurement of this ionization current
depends largely on the intensity of the current to be measured. If some
very active radium is spread on the lower of two insulated plates as in
Fig. 1, and a saturating electric field applied, the current may readily
be measured by a sensitive galvanometer of high resistance. For example,
a weight of ·45 gr. of radium chloride of activity 1000 times that of
uranium oxide, spread over a plate of area 33 sq. cms., gave a maximum
current of 1·1 × 10⁻⁸ amperes when the plates were 4·5 cms. apart. In
this case the difference of potential to be applied to produce practical
saturation was about 600 volts. Since most of the ionization is due to
rays which are absorbed in passing through a few centimetres of air, the
current is not much increased by widening the distance between the two
plates. In cases where the current is not quite large enough for direct
deflection, the current may be determined by connecting the upper
insulated plate with a well insulated condenser. After charging for a
definite time, say one or more minutes, the condenser is discharged
through the galvanometer, and the current can readily be deduced.
=55.= In most cases, however, when dealing with less active substances
like uranium or thorium, or with small amounts of active material, it is
necessary to employ methods for measuring much smaller currents than can
be detected conveniently by an ordinary galvanometer. The most
convenient apparatus to employ for this purpose is one of the numerous
types of quadrant electrometer or an electroscope of special design. For
many observations, especially where the activity of the two substances
is to be compared under constant conditions, an electroscope offers a
very certain and easy method of measurement. As an example of a simple
apparatus of this kind, a brief description will be given of the
electroscope used by M. and Mme Curie in many of their earlier
observations.
[Illustration: Fig. 11.]
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