Radioactive Decay Law

radioactive decay curve - plotThe radioactive decay law is an universal law that describes the statistical behaviour of a large number of nuclides.

As was written, radioactive decay is a random process at the level of single atoms, in that, according to quantum theory, it is impossible to predict when a particular atom will decay. In other words, a nucleus of a radionuclide has no “memory”. A nucleus does not “age” with the passage of time. Thus, the probability of its breaking down does not increase with time, but stays constant no matter how long the nucleus has existed. During its unpredictable decay this unstable nucleus spontaneosly and randomly decomposes to form a different nucleus (or a different energy state – gamma decay), giving off radiation in the form of atomic partices or high energy rays.

Calculations of the decay of radioactive nuclei are relatively straightforward, owing to the fact that there is only one fundamental law governing all decay process.

The radioactive decay law states that the probability per unit time that a nucleus will decay is a constant, independent of time. This constant is called the decay constant and is denoted by λ, “lambda”. This constant probability may vary greatly between different types of nuclei, leading to the many different observed decay rates. The radioactive decay of certain number of atoms (mass) is exponential in time.

Radioactive decay law: N = N.e-λt

The rate of nuclear decay is also measured in terms of half-lives. The half-life is the amount of time it takes for a given isotope to lose half of its radioactivity. If a radioisotope has a half-life of 14 days, half of its atoms will have decayed within 14 days. In 14 more days, half of that remaining half will decay, and so on. Half lives range from millionths of a second for highly radioactive fission products to billions of years for long-lived materials (such as naturally occurring uranium). Notice that short half lives go with large decay constants. Radioactive material with a short half life is much more radioactive (at the time of production) but will obviously lose its radioactivity rapidly. No matter how long or short the half life is, after seven half lives have passed, there is less than 1 percent of the initial activity remaining.

The radioactive decay law can be derived also for activity calculations or mass of radioactive material calculations:

(Number of nuclei) N = N.e-λt     (Activity) A = A.e-λt      (Mass) m = m.e-λt

, where N (number of particles) is the total number of particles in the sample, A (total activity) is the number of decays per unit time of a radioactive sample, m is the mass of remaining radioactive material.

Table of examples of half lives and decay constants.
Table of examples of half lives and decay constants. Notice that short half lives go with large decay constants. Radioactive material with a short half life is much more radioactive but will obviously lose its radioactivity rapidly.

Decay Constant and Half-Life

In calculations of radioactivity one of two parameters (decay constant or half-life), which characterize the rate of decay, must be known. There is a relation between the half-life (t1/2) and the decay constant λ. The relationship can be derived from decay law by setting N = ½ No. This gives:

where ln 2 (the natural log of 2) equals 0.693. If the decay constant (λ) is given, it is easy to calculate the half-life, and vice-versa.

Bateman Equations

Bateman EquationsIn physics, the Bateman equations are a set of first-order differential equations, which describe the time evolution of nuclide concentrations undergoing serial or linear decay chain. The model was formulated by Ernest Rutherford in 1905 and the analytical solution for the case of radioactive decay in a linear chain was provided by Harry Bateman in 1910. This model can be also used in nuclear depletion codes to solve nuclear transmutation and decay problems.

For example, ORIGEN is a computer code system for calculating the buildup, decay, and processing of radioactive materials. ORIGEN uses a matrix exponential method to solve a large system of coupled, linear, first-order ordinary differential equations (similar to the Bateman equations) with constant coefficients.

The Bateman equations for radioactive decay case of n – nuclide series in linear chain describing nuclide concentrations are as follows shown in the figure.

Example – Radioactive Decay Law

Iodine 131 - decay schemeA sample of material contains 1 mikrogram of iodine-131. Note that, iodine-131 plays a major role as a radioactive isotope present in nuclear fission products, and it a major contributor to the health hazards when released into the atmosphere during an accident. Iodine-131 has a half-life of 8.02 days.

Calculate:

  1. The number of iodine-131 atoms initially present.
  2. The activity of the iodine-131 in curies.
  3. The number of iodine-131 atoms that will remain in 50 days.
  4. The time it will take for the activity to reach 0.1 mCi.

Solution:

  1. The number of atoms of iodine-131 can be determined using isotopic mass as below.

NI-131 = mI-131 . NA / MI-131

NI-131 = (1 μg) x (6.02×1023 nuclei/mol) / (130.91 g/mol)

NI-131 = 4.6 x 1015 nuclei

  1. The activity of the iodine-131 in curies can be determined using its decay constant:

The iodine-131 has half-live of 8.02 days (692928 sec) and therefore its decay constant is:

Using this value for the decay constant we can determine the activity of the sample:

3) and 4) The number of iodine-131 atoms that will remain in 50 days (N50d) and the time it will take for the activity to reach 0.1 mCi can be calculated using the decay law:

As can be seen, after 50 days the number of iodine-131 atoms and thus the activity will be about 75 times lower. After 82 days the activity will be approximately 1200 times lower. Therefore, the time of ten half-lives (factor 210 = 1024) is widely used to define residual activity.

 

References:

Radiation Protection:

  1. Knoll, Glenn F., Radiation Detection and Measurement 4th Edition, Wiley, 8/2010. ISBN-13: 978-0470131480.
  2. Stabin, Michael G., Radiation Protection and Dosimetry: An Introduction to Health Physics, Springer, 10/2010. ISBN-13: 978-1441923912.
  3. Martin, James E., Physics for Radiation Protection 3rd Edition, Wiley-VCH, 4/2013. ISBN-13: 978-3527411764.
  4. U.S.NRC, NUCLEAR REACTOR CONCEPTS
  5. U.S. Department of Energy, Nuclear Physics and Reactor Theory. DOE Fundamentals Handbook, Volume 1 and 2. January 1993.

Nuclear and Reactor Physics:

  1. J. R. Lamarsh, Introduction to Nuclear Reactor Theory, 2nd ed., Addison-Wesley, Reading, MA (1983).
  2. J. R. Lamarsh, A. J. Baratta, Introduction to Nuclear Engineering, 3d ed., Prentice-Hall, 2001, ISBN: 0-201-82498-1.
  3. W. M. Stacey, Nuclear Reactor Physics, John Wiley & Sons, 2001, ISBN: 0- 471-39127-1.
  4. Glasstone, Sesonske. Nuclear Reactor Engineering: Reactor Systems Engineering, Springer; 4th edition, 1994, ISBN: 978-0412985317
  5. W.S.C. Williams. Nuclear and Particle Physics. Clarendon Press; 1 edition, 1991, ISBN: 978-0198520467
  6. G.R.Keepin. Physics of Nuclear Kinetics. Addison-Wesley Pub. Co; 1st edition, 1965
  7. Robert Reed Burn, Introduction to Nuclear Reactor Operation, 1988.
  8. U.S. Department of Energy, Nuclear Physics and Reactor Theory. DOE Fundamentals Handbook, Volume 1 and 2. January 1993.
  9. Paul Reuss, Neutron Physics. EDP Sciences, 2008. ISBN: 978-2759800414.

See above:

Radioactive Decay