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Introduction Radiometric
Introduction Radiometric
0 INTRODUCTION
Radioactivity involves the emission of particles and rays from atomic
nucleus. These emissions can serve different purposes such as military, electric
power generation, exploration and research. In this case we are limited to the use
of radioactive emission in research that has to do with the study of the earth
(including the environment). The radioactive method in geophysical prospecting
can be divided into two parts viz: (i) radiation which involves wave (rather than
particles that are corpuscular in nature) emanating from the nuclei of atoms; (ii)
emission of massive particles from the nuclei of atoms. While the former can be
employed for environmental studies, the latter can be used for the exploration of
minerals containing uranium. Both cases require the use of geophysical tools such
as Geiger counter and scintillation counters and therefore must be regarded as
geophysical methods.
Industrial prospecting involves radioactive logging of exploratory drill holes
and airborne surveys with oscillation counters. Emission of rays or particles from
the nucleus of an atom is the backbone of the radiometric method in geophysical
prospecting.
-e
n
+P
Figure 1: Atypical Atom made up of the nucleus and electrons which are negatively
charged and revolve round the nucleus; the nucleus consists of neutrons, n, which carry no
charge and are therefore neutral, and positively charged protons, P; the number of
electrons is equal to the number of protons, hence the typical Atom is electrically neutral.
In some nuclei the configuration of neutron and proton is unstable. Such nuclei are
radioactive. Many isotopes of elements with Z¿81 (or A¿ 206) are naturally
radioactive. Many more are more radioactive by artificial means (nuclear reactors,
particle accelerators). There are three naturally radioactive series: the uranium
series, the actinium series and the thorium series. The uranium series have nuclei
with mass numbers given by 4n + 2, where n is an integer. The actinium and
thorium series have mass numbers of type 4n + 3 and 4n respectively.
2.3 Nuclear Reaction
The electrostatics Coulomb force causes the protons to attract each other, and the
force decreases as the inverse square of the separation between the protons and so
can act over distances that are large compared to the size of the nucleus. Even
more powerful nuclear force holds the nucleus together. This attractive force acts
between protons, between neutrons, and between proton and neutron. It is only
effective at short distances, for a particle separation less than about 1 x 10-15 m.
Repulsion acts between every pair of protons in a nucleus, while the short-
range nuclear force acts only on nearby protons and neutrons. To avoid flying
apart due to Coulomb repulsion all nuclei with atomic number Z greater than about
20 have an excess of neutrons (N > Z). This helps to dilute the effects of the
repulsion-producing protons. However, nuclei with Z ≥ 83 are unstable and
disintegrate by radioactive decay; that is, they break up spontaneously by emitting
elementary particles (such as α and β) having masses, and other radiation (such as,
γ in form of wave or radiation) having no mass.
At least 28 distinct elementary particles are known to nuclear physics
(Lowrie, 1997). The most important ones are identified as α-particle (which
carries positive charge), β-particle (which carries negative charge), and γ-radiation
(which carries no charge, but has the speed of light). The unstable nucleus of
radioactive elements emits certain elementary particles or in some cases captures
an electron, to obtain stability. There are three different kinds of radiation, alpha,
beta and gamma.
Where 4.2 MeV (mega electron volts) is the difference in binding energy, or the
mass difference, between the parent element and its daughter. It is the kinetic
energy of the emitted α-particle. Most α-radiators are the heavy nuclei belonging
to the nuclides at the end of the periodic system. The majority have nuclei with A
˃ 200. One assumes that the lighter nuclei have α-decay times to be observable.
The α-particle is exceptionally stable, having a double magic number (2 protons
plus 2 neutrons). They behave like separate quantities, such as neutrons and
protons.
There are α-radiators which emit several groups of α-particles with distinctly
different range (i.e. energy). The explanation is that, when a nucleus emits an α-
particle with a kinetic energy, Eα , which is less than the maximum, the daughter
nucleus will be excited to a higher energy level. The excess energy, Δ Eα , will be
emitted as γ-radiation when the excited nucleus cascades down to its ground state.
The frequency v of the γ-radiation follows the hv = Δ Eα . It can also occur that the
parent nucleus is in an excited state when it emits α-particles. In that case the α-
particles will have a larger amount than normal range (i.e. energy).
Because α-particles have an electric charge, they ionize the matter through
which they pass. By the ionization they lose energy until they are slowed down
sufficiently to pick up two electrons and become a neural helium atom. Normally,
the range of α-particles is a few centimeters in the air and only some millimeters to
less than a millimeter in solids. Therefore it is possible to detect α-radiation in
prospecting. The α-radiation is of interest only because of the γ-radiation that goes
along with it.
where me is the electron mass, ( Ekin ¿e the kinetic energy of the electron, mv the
neutrino mass, ( Ekin ¿ v the kinetic energy of the neutrino mass, and c the velocity of
light in vacuum. E is the total energy. The kinetic energy of the emitted neutrino (
Ekin ¿ v changes in such a way with respect to the kinetic energy of the emitted
electron ( Ekin ¿e that the total energy e remains the same. ( Ekin ¿e Has its maximum
when ( Ekin ¿ v = 0.
The second remarkable fact is that before the emission of β-particle, the
nucleus contained no electrons nor neutrinos, but only neutrons and protons. This
is explained by the introduction of the “weak interaction” between protons and
neutrons. The weak interaction is a force resulting from the emission of an
electron, e- and a neutrino, v by the neutron, by which the neutron transforms
virtually into proton, p ̒, and the proton, p, by capturing these particles, transforms
into a neutron, n ̒. This can be represented by:
n + p (p ̒ + e ̄ + v) + p p ̒ + (e ̄ + v + p) p ̒ + n ̒.
This is to and fro motion of e ̄ and v, by which each time neutron and protein
exchange place, characterizes the weak interaction. For the β⁺ -emission we can
write similarly:
n + p n (e⁺ + v̅ + n ̒) (n + e⁺ + v̅) + n ̒ p ̒ + n ̒
where, v̅ is an antineutrino. The electron spin in these processes may either remain
with the charges e ̄ or e⁺ and change place with these charges or stay where they
were. In the first case we speak of a Majorana force, in the second case of
Heisenberg force. By assuming a potential U for the weak interaction, we have
U(r) =U 0 e−r /r 0
(15.8)
Some reactions emit additional energy in the form of γ-rays, which have a
very short wavelength and are similar in character to x-rays. γ -radiation consists of
high-energy photons, hence it is high-frequency radiation, as is apparent from the
relation ΔE = hv, where ΔE is spacing of the energy levels, h is Planck’s constant
and v is the frequency. For nuclear energy levels ΔE is the order of a MeV, which
is much larger than in atoms. γ -rays attenuate exponentially with distance from the
source. Normally they can be detected at distances up to several hundreds of
meters in air. In rock γ - rays are practically entirely absorbed within 0.5−¿2
meters, deepending on the type of rock, hard or sedimentary. It follows that
radioactive prospecting is limited to the same depth of 0.5−¿2 meters and is chiefly
concerned with the detection of γ -rays over radioactive ore bodies. As γ -rays are
products of the nuclei, they are not affected by the chemical form in which the
radioactive elements occur. Each isotope has its characteristic γ -ray spectrum. The
unit of radioactivity used in prospecting is micro-röntgen (r), which is the amount
of radiation producing 2.083 × 109 pairs of ions per cubic centimeter of air at
standard temperature and pressure (Gerkens, 1989). Also the count per minute is
used as a measure of radiation.
Of the radioactive element occurring in nature, we already mentioned the
uranium, the actinium and the thorium series. Also lighter radioactive isotopes are
found in nature. Of these the potassium isotope 40
K is of special interest in
prospecting. This isotope forms only a small percentage of the total amount of
potassium on earth, but it is widespread and contributes significantly to the
radioactivity of rocks. The respective content of U, Th, and K in rocks varies
strongly for different types of rocks. When rock undergoes weathering, the
radioactive elements contained in it are separated and are transported in different
ways. Thorium is not soluble in water and therefore can only be displaced by
mechanical processes. Uranium on the other hand occurs in easily soluble
compounds and migrates in watery solutions. It will therefore be found in the
remains of what used to be the liquid portion of the magma; an example is
pegmatite, commonly found as veins and dikes, and frequently associated
genetically with graphite. Also uranium can be found in sedimentary rock and
organic deposits. Of the sedimentary rock the clay has, in general, the largest and
the limestone the smallest concentration of radioactive isotopes (Gerkens, 1989) as
shown in Table 1.
Table 1: Concentration of radioactive isotopes in clay and limestone
in sedimentary rock (Adapted After Gerkens, 1989).
Content in Content in
Element Clay Limestone Remark
}
Radium 1.3 x 10 -12
0.5 x 10-12
Uranium 4.3 x 10-6 1.5 x 10-6 average values
in gram
Thorium 13.6 x 10-6 0.5 x 10-6
Potassium 3.0 x 10-2 0.1 x 10-2
Salt stones are not radioactive. Sandstones have a radioactive lying between that
of clay and limestone. Marine sediments are in general stronger radioactive than
terrestrial and estuarine sediments.
Suppose we have found a uranium deposit and we want to know whether its
exploitation is economically worthwhile, it must then have a certain minimum
percentage of U 3 O8 (usually taken to be 0.1%). In many cases only a chemical
analysis of samples can give the answer. If, however, we assume that the ore is in
equilibrium, that is when the creation of radioactive isotopes per second equals
their disintegration per second, and also we may assume that the ore is not
contaminated by other radioactive elements (such as Th or K), then a rough field
determination may be sufficient. With a “counter” the counts per minute of a
standard sample with known U 3 O8 content is compared with the counts of the field
sample.
If the field sample is contaminated by, for example, thorium (Th) or
potassium (K,) or when it is not in equilibrium, the count has to be corrected. To
determine the correction, the ratio of β- to γ -radiaion is measured by means of
counters. The ratio is known for the uranium series and by comparing the
measured with the known ratio the correction can be determined for either the
contamination or in the absence of contamination, for the not being in equilibrium
for the disintegration process.
During the disintegration, α and β particles are the pieces of the nucleus,
which are thrown out, while γ-rays are electromagnetic radiation, which often
accompany the ejection of α- and β-particles. For example, the radioactive element
radium-226 (226Ra) decays to radon-222 (222Rn) by α-particles emission as follows:
226
88 Ra →
222
86
4
Rn+ 2 He (i)
N t =N 0 e
−λt
(2.01)
N0 -
N, Activity (count)/s
½No
T½
Time, t
Figure 2: Exponential decay curve for a radioactive element
Each radioactive nuclide has its own “half-life” T 1/ 2 , in which the initial
number of parent nuclei is reduced to half this number, ½No; these are shown in
1
Figure 2. We find T 1/ 2 by putting Nt = 2 N 0 and t = T 1/ 2 in equation (2.01), giving:
¿ 2 0.693
T 1/ 2 = = λ (2.02)
λ
dN t
= −λ N 0 e− λt = −λ N t (2.03)
dt
We see that the rate of decay is proportional to the number of nuclei. The absolute
dN
value¿ dt ∨¿ is called the “activity” of the element and is expressed in curie (in
honour of Pierre and Marie Curie). The curie is defined as the activity of
radioactive matter decaying at a rate of 3.700 × 1010 nuclei per second (which is
about the activity of 1 g.Ra). Equations (2.01) and (2.0.3) are statistical laws, valid
only for nuclei with large numbers. Between the disintegration constant λ and the
half-life T ½ on one side and the range of the α-particles on the other side exists a
remarkable relation. Taking the logarithm of both sides of equation (2.02), we
obtain:
1 2
Replacing V by the kinetic energy Ea = 2 ma V (2.06)
log λ = A“ + B” log Ea
We see that there exists a linear relationship between log λ and log E. (According
to wave mechanical theory this is an approximation).