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Radio-Activity

Chapter 19: Secondary Rays.
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A systematic physical account examines the properties and behaviors of naturally radioactive substances, presenting the disintegration theory as a unifying explanation for spontaneous atomic change and decay chains. It reviews the ionization of gases and the electric, magnetic, and velocity properties of emitted radiation, describes alpha, beta, and gamma rays and emanations, and outlines experimental methods and quantitative measurement techniques. Additional chapters analyze successive transformations among radio-elements, summarize recent results on rays and emanations, and include appendices on alpha-ray studies and the occurrence and chemistry of radioactive minerals, with brief comments on physiological effects.

Fig. 35.

99. The α rays from different compounds of the same active element, although differing in amount, have about the same average penetrating power. Experiments on this point have been made by the writer[160] and by Owens[161]. Thus in comparing the relative power of penetration of the α rays from the different radio-elements, it is only necessary to determine the penetrating power for one compound of each of the radio-elements. Rutherford and Miss Brooks[162] have determined the amount of absorption of the α rays from the different active substances in their passage through successive layers of aluminium foil ·00034 cm. thick. The curves of absorption are given in Fig. 35. For the purpose of comparison in each case, the initial current with the bare active compound was taken as 100. A very thin layer of the active substance was used, and, in the case of thorium and radium, the emanations given off were removed by a slow current of air through the testing vessel. A potential difference of 300 volts was applied between the plates, which was sufficient to give the maximum current in each case.

Curves for the minerals organite and thorite were very nearly the same as for thoria.

For comparison, the absorption curves of the excited radiations of thorium and radium are given, as well as the curve for the radio-elements uranium, thorium, radium, and polonium. The α radiations may be arranged in the following order, as regards their power of penetration, beginning with the most penetrating.

Thorium}
Radium } excited radiation.
Thorium.
Radium.
Polonium.
Uranium.

The same order is observed for all the absorbing substances examined, viz., aluminium, Dutch metal, tinfoil, paper, and air and other gases. The differences in the absorption of the α rays from the active bodies are thus considerable, and must be ascribed either to a difference of mass or of velocity of the α particles or to a variation in both these quantities.

Since the α rays differ either in mass or velocity, it follows that they cannot be ascribed to any single radio-active impurity common to all radio-active bodies.

100. Absorption of the α rays by gases. The α rays from the different radio-active substances are quickly absorbed in their passage through a few centimetres of air at atmospheric pressure and temperature. In consequence of this, the ionization of the air, due to the α rays, is greatest near the surface of the radiating body and falls off very rapidly with the distance (see section 98).

Fig. 36.

A simple method of determining the absorption in gases is shown in Fig. 36. The maximum current is measured between two parallel plates A and B kept at a fixed distance of 2 cms. apart, and then moved by means of a screw to different distances from the radio-active surface. The radiation from this active surface passed through a circular opening in the plate A, covered with thin aluminium foil, and was stopped by the upper plate. For observations on other gases besides air, and for examining the effect at different pressures, the apparatus is enclosed in an air-tight cylinder.

If the radius of the active surface is large compared with the distance of the plate A from it, the intensity of the radiation is approximately uniform over the opening in the plate A, and falls off with the distance x traversed according to an exponential law. Thus

where λ is the “absorption constant” of the radiation for the gas under consideration[163]. Let

x = distance of lower plate from active material,
l = distance between the two fixed plates.

The energy of the radiation at the lower plate is then

and at the upper plate

The total number of ions produced between the parallel plates A and B is therefore proportional to

Since the factor

is a constant, the saturation current between A and B varies as

i.e. it decreases according to an exponential law with the distance traversed.

Fig. 37.

The variation of the current between A and B with the distance from a thin layer of uranium oxide is shown in Fig. 37 for different gases. The initial measurements were taken at a distance of about 3·5 mms. from the active surface. The actual values of this initial current were different for the different gases, but, for the purposes of comparison, the value is in each case taken as unity.

It will be seen that the current falls off with the distance approximately in a geometrical progression, a result which is in agreement with the simple theory given above. The distance through which the rays pass before they are absorbed is given below for different gases.

Gas Distance in mms. to absorb half of radiation
Carbonic acid 3
Air 4·3
Coal-gas 7·5
Hydrogen 16

The results for hydrogen are only approximate, as the absorption is small over the distance examined.

The absorption is least in hydrogen and greatest in carbonic acid, and follows the same order as the densities of the gases. In the case of air and carbonic acid, the absorption is proportional to the density, but this rule is widely departed from in the case of hydrogen. Results for the relative absorption by air of the α rays from the different active bodies are shown in Fig. 38.

Fig. 38.

The initial observation was made about 2 mms. from the active surface, and the initial current is in each case taken as 100. The current, as in the case of uranium, falls off at first approximately in geometrical progression with the distance. The thickness of air, through which the radiation passes before the intensity is reduced to half value, is given below.

Distance in mms.
Uranium 4·3
Radium 7·5
Thorium 10
Excited radiation from Thorium and Radium 16·5

The order of absorption by air of the radiations from the active substances is the same as the order of absorption by the metals and solid substances examined.

101. Connection between absorption and density. Since in all cases the radiations first diminish approximately according to an exponential law with the distance traversed, the intensity I after passing through a thickness x is given by

where λ is the absorption constant and I₀ the initial intensity.

The following table shows the value of λ with different radiations for air and aluminium.

Radiation λ for aluminium λ for air
Excited radiation 830 ·42
Thorium 1250 ·69
Radium 1600 ·90
Uranium 2750 1·6

Taking the density of air at 20° C. and 760 mms. as 0·00120 compared with water as unity, the following table shows the value of λ divided by density for the different radiations.

Radiation Aluminium Air
Excited radiation 320 350
Thorium 480 550
Radium 620 740
Uranium 1060 1300

Comparing aluminium and air, the absorption is thus roughly proportional to the density for all the radiations. The divergence, however, between the absorption-density numbers is large when two metals like tin and aluminium are compared. The value of λ for tin is not much greater than for aluminium, although the density is nearly three times as great.

If the absorption is proportional to the density, the absorption in a gas should vary directly as the pressure, and this is found to be the case. Some results on this subject have been given by the writer (loc. cit.) for uranium rays between pressures of ¼ and 1 atmosphere. Owens (loc. cit.) examined the absorption of the α radiation in air from thoria between the pressures of 0·5 to 3 atmospheres and found that the absorption varied directly as the pressure.

The variation of absorption with density for the projected positive particles is thus very similar to the law for the projected negative particles and for cathode rays. The absorption, in both cases, depends mainly on the density, but is not in all cases directly proportional to it. Since the absorption of the α rays in gases is probably mainly due to the exhaustion of the energy of the rays by the production of ions in the gas, it seems probable that the absorption in metals is due to a similar cause.

102. Relation between ionization and absorption in gases. It has been shown (section 45) that if the α rays are completely absorbed in a gas, the total ionization produced is about the same for all the gases examined. Since the rays are unequally absorbed in different gases, there should be a direct connection between the relative ionization and the relative absorption. This is seen to be the case if the results of Strutt (section 45) are compared with the relative absorption constants (section 100).

Gas Relative absorption Relative ionization
Air 1 1
Hydrogen ·27 ·226
Carbon dioxide 1·43 1·53

Considering the difficulty of obtaining accurate determinations of the absorption, the relative ionization in a gas is seen to be directly proportional to the relative absorption within the limits of experimental error. This result shows that the energy absorbed in producing an ion is about the same in air, hydrogen, and carbon dioxide.

103. Mechanism of the absorption of α rays by matter. The experiments, already described, show that the ionization of the gas, due to the α rays from a large plane surface of radio-active matter, falls off in most cases approximately according to an exponential law, until most of the rays are absorbed, whereupon the ionization decreases at a much faster rate. In the case of polonium, the ionization falls off more rapidly than is to be expected on the simple exponential law.

The ionization produced in the gas is due to the collision of the rapidly moving α particles with the molecules of the gas in their path. On account of its large mass, the α particle is a far more efficient ionizer than the β particle moving at the same speed. It can be deduced from the results of experiment that each projected α particle is able to produce about 100,000 ions in passing through a few centimetres of the gas before its velocity is reduced to the limiting value, below which it no longer ionizes the gas in its path.

Energy is required to ionize the gas, and this energy can only be obtained at the expense of the kinetic energy of the projected α particle. Thus it is to be expected that the α particle should gradually lose its velocity and energy of motion in its passage through the gas.

Since the rate of absorption of the α rays in gases is deduced from measurements of the ionization of the gas at different distances from the source of radiation, a knowledge of the law of variation of the ionizing power of the projected α particle with its speed is required in order to interpret the results. The experimental data on this question are, however, too incomplete to be applied directly to a solution of this question. Townsend[164] has shown that a moving electron produces ions in the gas after a certain limiting velocity is reached. The number of ions produced per centimetre of its path through the gas then rises to a maximum, and for still higher speeds continuously decreases. For example, Townsend found that the number of ions produced by an electron moving in an electric field was small at first for weak fields, but increased with the strength of the electric field to a maximum corresponding to the production of 20 ions per cm. of path in air at a pressure of 1 mm. of mercury. Durack[165] found that the electrons, generated in a vacuum tube, moving with a velocity of about 5 × 109 cms. per second produced a pair of ions every 5 cms. of path at 1 mm. pressure. In a later paper, Durack showed that for the electrons from radium, which are projected with a velocity greater than half the velocity of light, a pair of ions was produced every 10 cms. of path. The high speed electron from radium is thus a very inefficient ionizer and produces only about ¹⁄₁₀₀ of the ionization per unit path observed by Townsend for the slow moving electron.

104. In the case of the α particle, no direct measurements have been made upon the variation of the ionization with the velocity of the particle, so that the law of absorption of the rays cannot be deduced directly. An indirect attack upon the question has, however, been made recently by Bragg and Kleeman[166] who have formulated a simple theory to account for the experimental results which they have obtained upon the absorption of the α rays. The α particles from each simple type of radio-active matter are supposed to be projected with the same velocity, and to pass through a definite distance a in air at atmospheric pressure and temperature before they are all absorbed. As a first approximation the ionization per unit path is supposed to be the same over the whole length traversed before absorption, and to cease fairly suddenly at a definite distance from the source of radiation. This is in agreement with the observed fact that the ionization between parallel plates increases very rapidly when it approaches nearer than a certain distance to the radiant source. The range a depends upon the initial energy of motion of the α particle and will thus be different for different kinds of radio-active matter. If a thick layer of radio-active matter is employed, only the α particles from the surface have a range a. Those which reach the surface from a depth d have their range diminished by an amount ρd, where ρ is the density of the radio-active matter compared with air. This is merely an expression of the fact that the absorption of the α rays is proportional to the thickness and density of matter traversed. The rays from a thick layer of active matter will thus be complex, and will consist of particles of different velocity whose ranges have all values between 0 and a.

Suppose that a narrow pencil of α rays is emitted from a thick layer of radio-active material, and confined by metal stops as in Fig. 39.

Fig. 39.

The pencil of rays passes into an ionization vessel AB through a fine wire gauze A. The amount of ionization is to be determined between A and B for different distances h from the source of the rays R to the plate A.

All the particles coming from a depth x of the material given by h = a – ρx will enter the ionization vessel. The number of ions produced in a depth dh of the ionization vessel is equal to nxdh, i.e. to

ah
n ------ dh ,
ρ

where n is a constant.

If the depth of the ionization vessel be b, the total number of ions produced in the vessel is

This supposes that the stream of particles passes completely across the vessel. If not, the expression becomes

If the ionization in the vessel AB is measured, and a curve plotted showing its relation to h, the curve in the former case should be a straight line whose slope is nb/ρ and in the latter a parabola.

Thus if a thin layer of radio-active material is employed and a shallow ionization vessel, the ionization would be represented by a curve such as APM (Fig. 40), where the ordinates represent distances from the source of radiation, and the abscissae the ionization current between the plates AB.

Fig. 40.

In this case, PM is the range of the α particles from the lowest layer of the radio-active matter. The current should be constant for all distances less than PM.

For a thick layer of radio-active matter, the curve should be a straight line such as APB.

Curves of the above character should only be obtained when definite cones of rays are employed, and where the ionization vessel is shallow and includes the whole cone of rays. In such a case the inverse square law need not be taken into account.

In the experiments previously recorded (sections 99 and 100), the ionization was measured between parallel plates several centimetres apart for a large area of radio-active material. Such an arrangement was necessary at the time at which the experiments were made, as only weak radio-active material was available. Measurable electrical effects could not then be obtained with narrow cones of rays and shallow ionization vessels, but this disadvantage is removed by the advent of pure radium bromide as a source of radiation.

The interesting experiments described by Bragg and Kleeman show that the theoretical curves are approximately realized in practice. The chief difficulty experienced in the analysis of the experimental results was due to the fact that radium is a complex radio-active substance and contains four radio-active products each of which gives rise to α rays which have different ranges. The general character of the results obtained from radium are shown graphically in Fig. 41, curves A, B, C, D.

Fig. 41.

The ordinates represent the distance between the radium and the gauze of the testing vessel; the abscissae the current in the ionization vessel in arbitrary units. Five milligrams of radium bromide were used, and the depth of the ionization vessel was about 5 mms. Curve A is for a cone of rays of angle 20°. The initial current at a distance of 7 cms. is due to the β and γ rays and natural leak. This curve is initially parabolic, and then is made up of two straight lines. Curve B is for a smaller cone, and shows the straight line character of the curve to within a short distance of the radium. Curve C was obtained under the same condition as curve A, but with a layer of gold beater’s skin placed over the radium. The effect of this is to reduce all the ordinates of curve A by the same quantity. This is to be expected on the simple theory already considered. Curve D was obtained when the radium was heated so as to get rid of the emanation and its products. The α particles of greatest range are quite absent and the curve is simpler in character.

Fig. 42.

The complex character of the radium curves are more clearly brought out by a careful examination of a portion of the curve at distances between 2 and 5 cms. from the radium, using an ionization vessel of depth only 2 mms. The results are shown in Fig. 42, where the curve is seen to consist approximately of four straight lines of different slopes represented by PQ, QR, RS, ST.

Such a result is to be expected, for it will be shown later that four distinct α ray products exist in radium when in radio-active equilibrium. Each of these products of radium emits an equal number of α particles per second, but the range of each is different. If a1 is the range of one stream, a2 of another, the ionization in the vessel AB, when two streams enter the vessel, should be

 nb                 nb
---- (a1-h-b/2) + ----- (a2hb/2),
 ρ                 ρ

i.e.

 nb
---- (a1 + a2 – 2hb) .
ρ

Thus the slope of the curve should in this case be 2nb/ρ, while if only one stream enters, it should be nb/ρ. When three reach it, the slope should be 3nb/ρ and for four 4nb/ρ. These results are realized fairly closely in practice. The curve (Fig. 42) consists of four parts, whose slopes are in the proportion 16, 34, 45, 65, i.e. very nearly in the ratio 1, 2, 3, 4.

Experiments were also made with very thin layers of radium bromide, when, as we have seen (Fig. 40) a very different shape of curve is to be expected. An example of the results is shown in Fig. 43, curves I., II. and III. Curve I. is obtained from radium bromide which has been heated to drive off the emanation, and curves II. and III. from the same substance several days later, when the emanation was again accumulating. The portion PQ, which is absent in the first curve, is probably due to the “excited” activity produced by the emanation. By careful examination of the successive changes in the curves after the radium has been heated to drive off the emanation, it is possible to tell the range of the α rays from each of the different products, and this has been done to some extent by Bragg and Kleeman.

It will be seen later that the results here obtained support in a novel way the theory of radio-active changes which has been advanced from data of quite a different character.

The inward slope of the curve in Fig. 43 due to the radium indicates that the α particles become more efficient ionizers as their velocity decreases. This is in agreement with observations on the β rays. In some cases Bragg also observed that the α particles are the most efficient ionizers just before they lose their power of ionizing the gas.

Fig. 43.

Thus we may conclude from these experiments that the α particles from a simple radio-active substance traverse a definite distance in air, at a definite pressure and temperature, and that the ionization ends fairly abruptly. If the rays traverse a sheet of metal, the effective range of ionization is diminished by a distance corresponding to ρd, where ρ is the density of the material compared with air and d its thickness. The α rays from a thick layer of a simple radio-active substance consist of α particles of different velocities, which have ranges in air lying between 0 and the maximum range. The ionization of the particles per unit path is greatest near the end of its range, and decreases somewhat as we approach the radiant source. A complex source of rays like radium gives out four types of rays, each of which has a different but distinct range.

From this theory it is possible to calculate approximately the decrease of current to be observed when sheets of metal foil are placed over a large area of radio-active substance. This is the method that has been employed to obtain the curves of Figs. 35 and 38.

Suppose a very thin layer of simple radio-active matter is employed (for example a bismuth plate covered with radio-tellurium or a metal plate made active by exposure to the presence of the thorium or radium emanations) and that the ionization vessel is of sufficient depth to absorb the α rays completely.

Let d be the thickness of the metal plate, ρ its density compared with air. Consider a point P close to the upper side of the plate. The range of the particles moving from a point, when the path makes an angle θ with the normal at P, is a – ρd sec θ, where a is the range in air. The rays coming from points such that the paths make an angle with the normal greater than

will thus be absorbed in the plate. By integrating over the circular area under the point P, it is easy to show that the total ionization in the vessel is proportional to

The curves showing the relation between current and distance of metal traversed should thus be parabolic with respect to d. This is approximately the case for a simple substance like radio-tellurium. The curve for a thick layer of radium would be difficult to calculate on account of the complexity of the rays, but we know from experiment that it is approximately exponential. An account of some recent investigations made to determine the range of velocity over which the α particle is able to ionize the gas is given in Appendix A. The results there given strongly support the theory of absorption of the α rays discussed above.

PART IV.

The γ or very penetrating Rays.

105. In addition to the α and β rays, the three active substances, uranium, thorium, and radium, all give out a radiation of an extraordinarily penetrating character. These γ rays are considerably more penetrating than the X rays produced in a “hard” vacuum tube. Their presence can readily be observed for an active substance like radium, but is difficult to detect for uranium and thorium unless a large quantity of active material is used. Villard[167], using the photographic method, first drew attention to the fact that radium gave out these very penetrating rays, and found that they were non-deviable by a magnetic field. This result was confirmed by Becquerel[168].

Using a few milligrams of radium bromide, the γ rays can be detected in a dark room by the luminosity they excite in the mineral willemite or a screen of platinocyanide of barium. The α and β rays are completely absorbed by placing a thickness of 1 centimetre of lead over the radium, and the rays which then pass through the lead consist entirely of γ rays. The very great penetrating power of these rays is easily observed by noting the slight diminution of the luminosity of the screen when plates of metal several centimetres thick are placed between the radium and the screen. These rays also produce ionization in gases and are best investigated by the electrical method. The presence of the γ rays from 30 mgrs. of radium bromide can be observed in an electroscope after passing through 30 cms. of iron.

106. Absorption of the γ rays. In an examination of the active substances by the electrical method, the writer[169] found that both uranium and thorium gave out γ rays in amount roughly proportional to their activity. An electroscope of the type shown in Fig. 12 was employed. This was placed on a large lead plate ·65 cm. thick, the active substance being placed in a closed vessel beneath.

The discharge due to the natural ionization of the air in the electroscope was first observed. The additional ionization due to the active substance must be that produced by rays which have passed through the lead plate and the walls of the electroscope. The following table shows that the discharge due to these rays decreases approximately according to an exponential law with the thickness of lead traversed.

Thickness of lead Rate of discharge
·62 cms. 100
„ + ·64 cms. 67
„ + 2·86 „ 23
„ + 5·08 „ 8

Using 100 grs. of uranium and thorium, the discharge due to the rays through 1 cm. of lead was quite appreciable, and readily measured. The results showed that the amount of γ rays was about the same for equal weights of thorium and uranium oxides. The penetrating power was also about the same as for the radium rays.

Fig. 44.

The writer showed that the absorption of the γ rays from radium was approximately proportional to the density of the substance traversed. A more detailed examination of the absorption of these rays in various substances has been recently made by McClelland[170]. The curve (Fig. 44) shows the decrease of the ionization current in a testing vessel due to the β and γ rays with successive layers of lead. It is seen that the β rays are almost completely stopped by 4 mms. of lead; the ionization is then due entirely to the γ rays.

In order to leave no doubt that all the β rays were absorbed, the radium was covered with a thickness of 8 mms. of lead, and measurements of the coefficient of absorption λ were made for additional thicknesses. The average value of λ was calculated from the usual equation

where d is the thickness of matter traversed. The following table shows the value of λ, (I) for the first 2·5 mms. of matter traversed (after initially passing through 8 mms. of lead), (II) for the thickness 2·5 to 5 mms., (III) for 5 to 10 mms., (IV) 10 to 15 mms.

TABLE A.

Substance I II III IV
         
Platinum 1·167      
Mercury ·726 ·661 ·538 ·493
Lead ·641 ·563 ·480 ·440
Zinc ·282 ·266 ·248 ·266
Aluminium ·104 ·104 ·104 ·104
Glass ·087 ·087 ·087 ·087
Water ·034 ·034 ·034 ·034

In the above table, the absorption in aluminium, glass and water was too small to determine with accuracy the variation of λ with distance traversed. It will be observed that, for the denser substances, the coefficient of absorption decreases with the distance through which the rays have passed. This indicates that the rays are heterogeneous. The variation of λ is more marked in heavy substances.

Table B gives the values of λ divided by density for the above numbers. If the absorption were directly proportional to the density, the quotient would be the same in all cases.

TABLE B.

λ divided by density.

Substance I II III IV
         
Platinum ·054      
Mercury ·053 ·048 ·039 ·036
Lead ·056 ·049 ·042 ·037
Zinc ·039 ·037 ·034 ·033
Aluminium ·038 ·038 ·038 ·038
Glass ·034 ·034 ·034 ·034
Water ·034 ·034 ·034 ·034

The numbers in column I vary considerably, but the agreement becomes closer in the succeeding columns, until in column IV the absorption is very nearly proportional to the density.

It is seen that the absorption of all three types of rays from radio-active substances is approximately proportional to the density of the substance traversed—a relation first observed by Lenard for the cathode rays. This law of absorption thus holds for both positively and negatively electrified particles projected from the radio-active substances, and also for the electromagnetic pulses which are believed to constitute the γ rays; although the absorption of the α rays, for example, is 10,000 times greater than for the γ rays. We have seen in section 84 that the value of the absorption constant λ for lead is 122 for the β rays from uranium. The value for the γ rays from radium varies between ·64 and ·44, showing that the γ rays are more than 200 times as penetrating as the β rays.

107. Nature of the rays. In addition to their great penetrating power, the γ rays differ from the α and β rays in not being deflected to an appreciable degree by a magnetic or electric field. In a strong magnetic field, it can be shown, using the photographic method, that there is an abrupt discontinuity between the β and γ rays, for the former are bent completely away from the latter. This indicates that, as regards the action of a magnetic field, there is no gradual transition of magnetic properties between the β and γ rays. Paschen[171] has examined the γ rays in a very intense magnetic field, and, from the absence of deflection of these rays, has calculated that, if they consist of electrified particles carrying an ionic charge, and projected with a velocity approaching that of light, their apparent mass must be at least 45 times greater than that of the hydrogen atom.

It now remains for us to consider whether the γ rays are corpuscular in character, or whether they are a type of electromagnetic pulse in the ether similar to Röntgen rays. They resemble Röntgen rays in their great penetrating power and in their absence of deflection in a magnetic field. Earlier experiments seemed to indicate an important difference between the action of γ and X rays. It is well known that ordinary X rays produce much greater ionization in gases such as sulphuretted hydrogen and hydrochloric acid gas, than in air, although the differences in density are not large. For example, exposed to X rays, sulphuretted hydrogen has six times the conductivity of air, while with γ rays the conductivity only slightly exceeds that of air. The results obtained by Strutt, in this connection, have already been given in section 45. It is there shown that the relative conductivity of gases exposed to γ rays (and also to α and β rays) is, in most cases, nearly proportional to their relative densities; but, under X rays, the relative conductivity for some gases and vapours is very much greater than for the γ rays. It must be remembered, however, that the results obtained by Strutt were for “soft X rays,” whose penetrating power was very much less than that of the γ rays. In order to see if the relative conductivity of gases produced by X rays depended upon their penetrating power, A. S. Eve[172] made some experiments with a very “hard” X ray bulb, which gave an unusually penetrating type of rays.

The results of the measurements are shown in the table below, where the conductivity for each type of rays is expressed relative to air as unity. The results obtained for “soft” X rays by Strutt and by Eve for γ rays are added for comparison.

It is seen that the hard rays show a much closer agreement than the soft rays with the density law found for the γ rays. The high values previously obtained for the vapours of chloroform and carbon tetrachloride are greatly reduced, and are very nearly the same as for the γ rays. On the other hand, the vapour of methyl iodide is an exception, and still shows a high conductivity. The γ rays were, however, forty times as penetrating as the hard X rays, and it is probable that the value of methyl iodide would be reduced with still more penetrating X rays.

Relative conductivities of gases.

Gas Relative Density “Soft” X rays “Hard” X rays γ rays
         
Hydrogen ·07 ·11 ·42 ·19
Air 1·0 1·0 1·0 1·0
Sulphuretted Hydrogen 1·2 6 ·9 1·23
Chloroform 4·3 32 4·6 4·8
Methyl Iodide 5·0 72 13·5 5·6
Carbon Tetrachloride 5·3 45 4·9 5·2

The hard X rays were found to give far more secondary radiation than the γ rays, but this effect is probably also a function of the penetrating power of the primary rays. It will be seen later (section 112) that γ rays give rise to a secondary radiation of the β ray type. This has also been observed for the X rays.

Considering the experimental evidence as a whole, there is undoubtedly a very marked similarity between the properties of γ and X rays. The view that the γ rays are a type of very penetrating X rays, also receives support from theoretical considerations. We have seen (section 52) that the X rays are believed to be electromagnetic pulses, akin in some respects to short light waves, which are set up by the sudden stoppage of the cathode ray particles. Conversely, it is also to be expected that X rays will be produced at the sudden starting, as well as at the sudden stopping, of electrons. Since most of the β particles from radium are ejected from the radium atom with velocities much greater than the cathode particles in a vacuum tube, X rays of a very penetrating character will arise. But the strongest argument in support of this view is derived from an examination of the origin and connection of the β and γ rays from radio-active substances. It will be shown later that the α ray activity observed in radium arises from several disintegration products, stored up in the radium, while the β and γ rays arise only from one of these products named radium C. It is found, too, that the activity measured by the γ rays is always proportional to the activity measured by the β rays, although by separation of the products the activity of the latter may be made to undergo great variations in value.

Thus the intensity of the γ rays is always proportional to the rate of expulsion of β particles, and this result indicates that there is a close connection between the β and γ rays. Such a result is to be expected if the β particle is the parent of the γ ray, for the expulsion of each electron from radium will give rise to a narrow spherical pulse travelling from the point of disturbance with the velocity of light.

108. There is another possible hypothesis in regard to the nature of these rays. It has been shown (sections 48 and 82) that the apparent mass of an electron increases as the speed of light is approached; theoretically it should be very great when the velocity of the electron is exceedingly close to the velocity of light. In such a case, a moving electron would be difficult to deflect by a magnetic or electric field.

The view that the γ rays are electrons carrying a negative charge and moving with a velocity nearly equal to that of light has recently been advocated by Paschen[173]. He concluded from experiment that the γ rays like the β rays carried a negative charge. We have seen (section 85) that Seitz also observed that a small negative charge was communicated to bodies on which the γ rays impinged, but the magnitude of this charge was much smaller than that observed by Paschen. I do not think that much weight can be attached to observations that a small positive or negative charge is communicated to bodies on which the γ rays fall, for it will be shown later that a strong secondary radiation, consisting in part of electrons, is set up during the passage of the γ rays through matter. It is not improbable that the small charge observed is not a direct result of the charge carried by the γ rays, but is an indirect effect due to the secondary radiations emitted from the surface of bodies. There is no doubt that a thick lead vessel, completely enclosing a quantity of radium, acquires a small positive charge, but this result would follow whether the γ rays carry a charge or not, since the secondary radiations from the lead surface consist of projected particles which carry with them a negative charge.

On this corpuscular theory of the nature of the γ rays, each electron must have a large apparent mass, or otherwise it would be appreciably deflected by an intense magnetic field. The energy of motion of the electron must, in consequence, be very great, and, if the number of the electrons constituting the γ rays is of the same order of magnitude as the number of the β particles, a large heating effect is to be expected when the γ rays are stopped in matter. Paschen[174] made some experiments on the heat emission of radium due to the γ rays; he concluded that the γ rays were responsible for more than half of the total heat emission of radium and carried away energy at the rate of over 100 gram calories per hour per gram of radium. This result was not confirmed by later experiments of Rutherford and Barnes[175], who found that the heating effect of the γ rays could not be more than a few per cent. of the total heat emission of radium. These results will be considered later in chapter XII.

The weight of evidence, both experimental and theoretical, at present supports the view that the γ rays are of the same nature as the X rays but of a more penetrating type. The theory that the X rays consist of non-periodic pulses in the ether, set up when the motion of electrons is arrested, has found most favour, although it is difficult to provide experimental tests to decide definitely the question. The strongest evidence in support of the wave nature of the X rays is derived from the experiments of Barkla[176], who found that the amount of secondary radiation set up by the X rays on striking a metallic surface depended on the orientation of the X ray bulb. The rays thus showed evidence of a one-sidedness or polarization which is only to be expected if the rays consist of a wave motion in the ether.

PART V.

Secondary Rays.

109. Production of secondary rays. It has long been known that Röntgen rays, when they impinge on solid obstacles, produce secondary rays of much less penetrating power than the incident rays. This was first shown by Perrin and has been investigated in detail by Sagnac, Langevin, Townsend and others. Thus it is not surprising that similar phenomena should be observed for the radiation from radio-active substances. By means of the photographic method, Becquerel[177] has made a close study of the secondary radiations produced by radio-active substances. In his earliest observations, he noticed that radiographs of metallic objects were always surrounded by a diffuse border. This effect is due to the secondary rays set up by the incident rays at the surface of the screen.

The secondary rays produced by the α rays are very feeble. They are best shown by polonium, which gives out only α rays, so that the results are not complicated by the action of the β rays. Strong secondary rays are set up at the point of impact of the β or cathodic rays. Becquerel found that the magnitude of this action depended greatly on the velocity of the rays. The rays of lowest velocity gave the most intense secondary action, while the penetrating rays gave, in comparison, scarcely any secondary effect. In consequence of the presence of this secondary radiation, the photographic impression of a screen pierced with holes is not clear and distinct. In each case there is a double photographic impression, due to the primary rays and the secondary rays set up by them.

These secondary rays are deviable by a magnetic field, and in turn produce tertiary rays and so on. The secondary rays are in all cases more readily deviated and absorbed than the primary rays, from which they arise. The very penetrating γ rays give rise to secondary rays, which cause intense action on the photographic plate. When some radium was placed in a cavity inside a deep lead block, rectangular in shape, besides the impression due to the direct rays through the lead, Becquerel observed that there was also a strong impression due to the secondary rays emitted from the surface of the lead. The action of these secondary rays on the plate is so strong that the effect on the plate is, in many cases, increased by adding a metal screen between the active material and the plate.

The comparative photographic action of the primary and secondary rays cannot be taken as a relative measure of the intensity of their radiations. For example, only a small portion of the energy of the β rays is in general absorbed in the sensitive film. Since the secondary rays are far more easily absorbed than the primary rays, a far greater proportion of their energy is expended in producing photographic action than in the case of the primary rays. It is thus not surprising that the secondary rays set up by the β and γ rays may in some cases produce a photographic impression comparable with, if not greater than, the effect of the incident rays.

On account of these secondary rays, radiographs produced by the β rays of radium in general show a diffuse border round the shadow of the object. For this reason radiographs of this kind lack the sharpness of outline of X ray photographs.

110. Secondary radiation produced by α rays. Mme Curie[178] has shown by the electric method that the α rays of polonium produce secondary rays. The method adopted was to compare the ionization current between two parallel plates, when two screens of different material, placed over the polonium, were interchanged.

These results show that the α rays of polonium are modified in passing through matter, and that the amount of secondary rays set up varies with screens of different material. Mme Curie, using the same method, was unable to observe any such effect for the β rays of radium. The production of secondary rays by the β rays of radium is, however, readily shown by the photographic method. We have already seen (section 93) that very low velocity electrons accompany the α rays from radium or radio-tellurium spread on a metal plate. These electrons are probably liberated when the α rays escape from or impinge upon matter, and the number emitted depends upon the kind of matter used as a screen. The differences shown in the above table when the screens were interchanged are explained simply in this way.

Screens employed Thickness in mms. Current observed
     
Aluminium 0·01  
Cardboard 0·005 17·9
     
Cardboard 0·005  
Aluminium 0·01 6·7
     
Aluminium 0·01  
Tin 0·005 150
     
Tin 0·005  
Aluminium 0·01 126
     
Tin 0·005  
Cardboard 0·005 13·9
     
Cardboard 0·005  
Tin 0·005 4·4