.

Radioactive decay, also known as nuclear decay or radioactivity, is the process by which a nucleus of an unstable atom loses energy by emitting ionizing radiation. A material that spontaneously emits this kind of radiation — which includes alpha particles, beta particles, gamma rays and conversion electrons — is considered radioactive.

Radioactive decay is a stochastic (i.e. 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.[1][2][3][4] The chance that a given atom will decay never changes, that is, it does not matter how long the atom has existed. For a large collection of atoms however, the decay rate for that collection can be calculated from their measured decay constants or half-lives. The half-lives of radioactive atoms have no known limits for shortness or length of duration, and range over 55 orders of magnitude in time.

There are many types of radioactive decay (see table below). A decay, or loss of energy, results when an atom with one type of nucleus, called the parent radionuclide (or parent radioisotope[note 1]), transforms into an atom with a nucleus in a different state, or with a nucleus containing a different number of protons and neutrons. The product is called the daughter nuclide. In some decays, the parent and the daughter nuclides are different chemical elements, and thus the decay process results in the creation of an atom of a different element. This is known as a nuclear transmutation.

The first decay processes to be discovered were alpha decay, beta decay, and gamma decay. Alpha decay occurs when the nucleus ejects an alpha particle (helium nucleus). This is the most common process of emitting nucleons, but in rarer types of decays, nuclei can eject protons, or in the case of cluster decay specific nuclei of other elements. Beta decay occurs when the nucleus emits an electron or positron and a neutrino, in a process that changes a proton to a neutron or the other way about. The nucleus may capture an orbiting electron, causing a proton to convert into a neutron in a process called electron capture. All of these processes result in a nuclear transmutation.

Alpha particles may be completely stopped by a sheet of paper, beta particles by aluminum shielding. Gamma rays can only be reduced by much more substantial barriers, such as a very thick layer of lead.

By contrast, there are radioactive decay processes that do not result in a nuclear transmutation. The energy of an excited nucleus may be emitted as a gamma ray in a process called gamma decay, or be used to eject an orbital electron by its interaction with the excited nucleus, in a process called internal conversion. Highly excited neutron-rich nuclei, formed as the product of other types of decay, occasionally lose energy by way of neutron emission, resulting in a change of an element from one isotope to another. Another type of radioactive decay results in products that are not defined, but appear in a range of "pieces" of the original nucleus. This decay, called spontaneous fission, happens when a large unstable nucleus spontaneously splits into two (and occasionally three) smaller daughter nuclei, and generally leads to the emission of gamma rays, neutrons, or other particles from those products.

For a summary table showing the number of stable and radioactive nuclides in each category, see radionuclide. There exist twenty-eight chemical elements on Earth that are radioactive. They are those that contain thirty-four radionuclides that date before the time of formation of the solar system. Well-known examples are uranium and thorium, but also included are naturally occurring long-lived radioisotopes such as potassium-40. Another fifty or so shorter-lived radionuclides, such as radium and radon, found on Earth, are the products of decay chains that began with the primordial nuclides, and ongoing cosmogenic processes, such as the production of carbon-14 from nitrogen-14 by cosmic rays. Radionuclides may also be produced artificially in particle accelerators or nuclear reactors, resulting in 650 of these with half-lives of over an hour, and several thousand more with even shorter half-lives. See this list of nuclides for a list by half life.

History of discovery
Pierre and Marie Curie in their Paris laboratory, before 1907

Radioactivity was discovered in 1896 by the French scientist Henri Becquerel, while working with phosphorescent materials.[5] These materials glow in the dark after exposure to light, and he suspected that the glow produced in cathode ray tubes by X-rays might be associated with phosphorescence. He wrapped a photographic plate in black paper and placed various phosphorescent salts on it. All results were negative until he used uranium salts. The uranium salts caused a blackening of the plate in spite of the plate being wrapped in black paper. These radiations were given the name "Becquerel Rays".

It soon became clear that the blackening of the plate had nothing to do with phosphorescence, as the blackening was also produced by non-phosphorescent salts of uranium and metallic uranium. It became clear from these experiments that there was a form of invisible radiation that could pass through paper and was causing the plate to react as if exposed to light.

At first, it seemed as though the new radiation was similar to the then recently discovered X-rays. Further research by Becquerel, Ernest Rutherford, Paul Villard, Pierre Curie, Marie Curie, and others showed that this form of radioactivity was significantly more complicated. Rutherford was the first to realize that all such elements decay in accordance with the same mathematical exponential formula. Rutherford and his student Frederick Soddy were the first to realize that many decay processes resulted in the transmutation of one element to another. Subsequently, the radioactive displacement law of Fajans and Soddy was formulated to describe the products of alpha and beta decay.[6][7]

The early researchers also discovered that many other chemical elements, besides uranium, have radioactive isotopes. A systematic search for the total radioactivity in uranium ores also guided Pierre and Marie Curie to isolate two new elements: polonium and radium. Except for the radioactivity of radium, the chemical similarity of radium to barium made these two elements difficult to distinguish.

Early health dangers
Taking an X-ray image with early Crookes tube apparatus in 1896. The Crookes tube is visible in the centre. The standing man is viewing his hand with a fluoroscope screen; this was a common way of setting up the tube. No precautions against radiation exposure are being taken; its hazards were not known at the time.

The dangers of ionizing radiation due to radioactivity and X-rays were not immediately recognized.
X-rays

The discovery of x‑rays in 1895 led to widespread experimentation by scientists, physicians, and inventors. Many people began recounting stories of burns, hair loss and worse in technical journals as early as 1896. In February of that year, Professor Daniel and Dr. Dudley of Vanderbilt University performed an experiment involving X-raying Dudley's head that resulted in his hair loss. A report by Dr. H.D. Hawks, of his suffering severe hand and chest burns in an X-ray demonstration, was the first of many other reports in Electrical Review.[8]

Other experimenters including Elihu Thomson, and Nikola Tesla also reported burns. Thomson deliberately exposed a finger to an X-ray tube over a period of time and suffered pain, swelling, and blistering.[9] Other effects, including ultraviolet rays and ozone were sometimes blamed for the damage,[10] and many physicians still claimed that there were no effects from X-ray exposure at all.[9]

Despite this, there were some early systematic hazard investigations, and as early as 1902 William Herbert Rollins wrote almost despairingly that his warnings about the dangers involved in careless use of X-rays was not being heeded, either by industry or by his colleagues. By this time Rollins had proved that X-rays could kill experimental animals, could cause a pregnant guinea pig to abort, and that they could kill a fetus.[11] He also stressed that "animals vary in susceptibility to the external action of X-light" and warned that these differences be considered when patients were treated by means of X-rays.

Radioactive substances

However, the biological effects of radiation due to radioactive substances were less easy to gauge. This gave the opportunity for many physicians and corporations to market radioactive substances as patent medicines. Examples were radium enema treatments, and radium-containing waters to be drunk as tonics. Marie Curie protested against this sort of treatment, warning that the effects of radiation on the human body were not well understood. Curie later died from aplastic anaemia, likely caused by exposure to ionizing radiation. By the 1930s, after a number of cases of bone necrosis and death of radium treatment enthusiasts, radium-containing medicinal products had been largely removed from the market (radioactive quackery).

Radiation protection
Main article: Radiation protection
See also: Sievert and Ionizing radiation

Only a year after Röntgen's discovery of X rays, the American engineer Wolfram Fuchs (1896) gave what is probably the first protection advice, but it was not until 1925 that the first International Congress of Radiology (ICR) was held and considered establishing international protection standards. The effects of radiation on genes, including the effect of cancer risk, were recognized much later. In 1927, Hermann Joseph Muller published research showing genetic effects and, in 1946, was awarded the Nobel prize for his findings.

The second ICR was held in Stockholm in 1928 and proposed the adoption of the rontgen unit, and the 'International X-ray and Radium Protection Committee' (IXRPC) was formed. Rolf Sievert was named Chairman, but a driving force was George Kaye of the British National Physical Laboratory. The committee met in 1931, 1934 and 1937.

After World War 2 the increased range and quantity of radioactive substances being handled as a result of military and civil nuclear programmes led to large groups of occupational workers and the public being potentially exposed to harmful levels of ionising radiation. This was considered at the first post-war ICR convened in London in 1950, when the present International Commission on Radiological Protection (ICRP) was born.[12] Since then the the ICRP has developed the present international system of radiation protection, covering all aspects of radiation hazard.
Units of radioactivity
Graphic showing relationships between radioactivity and detected ionizing radiation

The International System of Units (SI) unit of radioactive activity is the becquerel (Bq), named in honour of the scientist Henri Becquerel. One Bq is defined as one transformation (or decay or disintegration) per second.

An older unit of radioactivity is the curie, Ci, which was originally defined as the amount of radium emanation (radon-222) in equilibrium with one gram of pure radium, isotope Ra-226. Today, the curie is defined as the quantity of any radionuclide undergoing 3.7×1010 Bq disintegrations per second, so that 1 curie (Ci) = 3.7×1010 Bq. For radiological protection purposes, although the United States Nuclear Regulatory Commission permits the use of the unit curie alongside SI units,[13] the European Union European units of measurement directives required that its use for "public health ... purposes" be phased out by 31 December 1985.[14]

Types of decay
Alpha particles may be completely stopped by a sheet of paper, beta particles by aluminium shielding. Gamma rays can only be reduced by much more substantial mass, such as a very thick layer of lead.

Early researchers found that an electric or magnetic field could split radioactive emissions into three types of beams. The rays were given the names alpha, beta, and gamma, in order of their ability to penetrate matter. While alpha decay was seen only in heavier elements of atomic number 52 (tellurium) and greater, the other two types of decay were produced by of the elements. Lead, atomic number 82, is the heaviest element to have any isotopes stable (to the limit of measurement) to radioactive decay. Radioactive decay is seen in all isotopes of all elements of atomic number 83 (bismuth) or greater. Bismuth, however, is only very slightly radioactive.
Transition diagram for decay modes of a radionuclide, with neutron number N and atomic number Z (shown are α, β±, p+, and n0 emissions, EC denotes electron capture).
Types of radioactive decay related to N and Z numbers

In analysing the nature of the decay products, it was obvious from the direction of the electromagnetic forces applied to the radiations by external magnetic and electric fields that alpha particles carried a positive charge, beta particles carried a negative charge, and gamma rays were neutral. From the magnitude of deflection, it was clear that alpha particles were much more massive than beta particles. Passing alpha particles through a very thin glass window and trapping them in a discharge tube allowed researchers to study the emission spectrum of the captured particles, and ultimately proved that alpha particles are helium nuclei. Other experiments showed beta radiation, resulting from decay and cathode rays, were high-speed electrons. Likewise, gamma radiation and X-rays were found to be high-energy electromagnetic radiation.

The relationship between the types of decays also began to be examined: For example, gamma decay was almost always found to be associated with other types of decay, and occurred at about the same time, or afterwards. Gamma decay as a separate phenomenon, with its own half-life (now termed isomeric transition), was found in natural radioactivity to be a result of the gamma decay of excited metastable nuclear isomers, which were in turn created from other types of decay.

Although alpha, beta, and gamma radiations were most commonly found, other types of emission were eventually discovered. Shortly after the discovery of the positron in cosmic ray products, it was realized that the same process that operates in classical beta decay can also produce positrons (positron emission). In an analogous process, instead of emitting positrons and neutrinos, some proton-rich nuclides were found to capture their own atomic electrons, a process called electron capture, and subsequently emit only a neutrino and usually also a gamma ray. Each of these types of decay involves the capture or emission of nuclear electrons or positrons, and acts to move a nucleus toward the ratio of neutrons to protons that has the least energy for a given total number of nucleons, consequently producing a more stable nucleus.

A theoretical process of positron capture, analogous to electron capture, is possible in antimatter atoms, but has not been observed as the required antimatter atoms are not available.[15] This would require antimatter atoms at least as complex as beryllium-7, which is the lightest known isotope of normal matter to undergo decay by electron capture.

Shortly after the discovery of the neutron in 1932, Enrico Fermi realized that certain rare beta-decay reactions immediately yield neutrons as a decay particle (neutron emission). Isolated proton emission was eventually observed in some elements. It was also found that some heavy elements may undergo spontaneous fission into products that vary in composition. In a phenomenon called cluster decay, specific combinations of neutrons and protons other than alpha particles (helium nuclei) were found to be spontaneously emitted from atoms.

Other types of radioactive decay of different mechanisms were found to emit previously-seen particles. An example is internal conversion, which results in electron and sometimes high-energy photon emission, although it involves neither beta nor gamma decay. A neutrino is not emitted, and neither the electron nor photon originate in the nucleus. Internal conversion decay, like isomeric transition gamma decay and neutron emission, involves the release of energy by an excited nuclide, without the transmutation of one element into another.

Rare events that involve a combination of two beta-decay type events happening simultaneously are known (see below). Any decay process that does not violate the conservation of energy or momentum laws (and perhaps other particle conservation laws) is permitted to happen, although not all have been detected. An interesting example discussed in a final section, is bound state beta decay of rhenium-187. In this process, an inverse of electron capture, beta electron-decay of the parent nuclide is not accompanied by beta electron emission, because the beta particle has been captured into the K-shell of the emitting atom. An antineutrino, however, is emitted.

Radionuclides can undergo a number of different reactions. These are summarized in the following table. A nucleus with mass number A and atomic number Z is represented as (A, Z). The column "Daughter nucleus" indicates the difference between the new nucleus and the original nucleus. Thus, (A − 1, Z) means that the mass number is one less than before, but the atomic number is the same as before.

If energy circumstances are favorable, a given radionuclide may undergo many competing types of decay, with some atoms decaying by one route, and others decaying by another. An example is copper-64, which has 29 protons, and 35 neutrons, which decays with a half-life of about 12.7 hours. This isotope has one unpaired proton and one unpaired neutron, so either the proton or the neutron can decay to the opposite particle. This particular nuclide (though not all nuclides in this situation) is almost equally likely to decay through proton decay, producing a positron emission (18%), or through electron capture (43%), as it does through neutron decay by electron emission (39%). The excited energy states resulting from these decays which fail to end in a ground energy state, also produce later internal conversion and gamma decay in almost 0.5% of the time.

Mode of decay	Participating particles	Daughter nucleus
Decays with emission of nucleons:
Alpha decay	An alpha particle (A = 4, Z = 2) emitted from nucleus	(A − 4, Z − 2)
Proton emission	A proton ejected from nucleus	(A − 1, Z − 1)
Neutron emission	A neutron ejected from nucleus	(A − 1, Z)
Double proton emission	Two protons ejected from nucleus simultaneously	(A − 2, Z − 2)
Spontaneous fission	Nucleus disintegrates into two or more smaller nuclei and other particles	—
Cluster decay	Nucleus emits a specific type of smaller nucleus (A1, Z1) which is larger than an alpha particle	(A − A1, Z − Z1) + (A1, Z1)
Different modes of beta decay:
β− decay	A nucleus emits an electron and an electron antineutrino	(A, Z + 1)
Positron emission (β+ decay)	A nucleus emits a positron and an electron neutrino	(A, Z − 1)
Electron capture	A nucleus captures an orbiting electron and emits a neutrino; the daughter nucleus is left in an excited unstable state	(A, Z − 1)
Bound state beta decay	A free neutron or nucleus beta decays to electron and antineutrino, but the electron is not emitted, as it is captured into an empty K-shell; the daughter nucleus is left in an excited and unstable state. This process is a minority of free neutron decays (0.0004%) due to the low energy of hydrogen ionization, and is suppressed except in ionized atoms that have K-shell vacancies.	(A, Z + 1)
Double beta decay	A nucleus emits two electrons and two antineutrinos	(A, Z + 2)
Double electron capture	A nucleus absorbs two orbital electrons and emits two neutrinos – the daughter nucleus is left in an excited and unstable state	(A, Z − 2)
Electron capture with positron emission	A nucleus absorbs one orbital electron, emits one positron and two neutrinos	(A, Z − 2)
Double positron emission	A nucleus emits two positrons and two neutrinos	(A, Z − 2)
Transitions between states of the same nucleus:
Isomeric transition	Excited nucleus releases a high-energy photon (gamma ray)	(A, Z)
Internal conversion	Excited nucleus transfers energy to an orbital electron, which is subsequently ejected from the atom	(A, Z)

Radioactive decay results in a reduction of summed rest mass, once the released energy (the disintegration energy) has escaped in some way. Although decay energy is sometimes defined as associated with the difference between the mass of the parent nuclide products and the mass of the decay products, this is true only of rest mass measurements, where some energy has been removed from the product system. This is true because the decay energy must always carry mass with it, wherever it appears (see mass in special relativity) according to the formula E = mc2. The decay energy is initially released as the energy of emitted photons plus the kinetic energy of massive emitted particles (that is, particles that have rest mass). If these particles come to thermal equilibrium with their surroundings and photons are absorbed, then the decay energy is transformed to thermal energy, which retains its mass.

Decay energy therefore remains associated with a certain measure of mass of the decay system, called invariant mass, which does not change during the decay, even though the energy of decay is distributed among decay particles. The energy of photons, the kinetic energy of emitted particles, and, later, the thermal energy of the surrounding matter, all contribute to the invariant mass of the system. Thus, while the sum of the rest masses of the particles is not conserved in radioactive decay, the system mass and system invariant mass (and also the system total energy) is conserved throughout any decay process. This is a restatement of the equivalent laws of conservation of energy and conservation of mass.
Radioactive decay rates

The decay rate, or activity, of a radioactive substance is characterized by:

Constant quantities:

• The half-life—t_1/2, is the time taken for the activity of a given amount of a radioactive substance to decay to half of its initial value; see List of nuclides.
• The decay constant— λ, "lambda" the inverse of the mean lifetime, sometimes referred to as simply decay rate.
• The mean lifetime— τ, "tau" the average lifetime of a radioactive particle before decay.

Although these are constants, they are associated with statistically random behaviour of populations of atoms. In consequence, predictions using these constants are less accurate for small number of atoms.

In principle a half-life, a third-life, or even a (1/√2)-life, can be used in exactly the same way as half-life; but the mean life and half-life t1/2 have been adopted as standard times associated with exponential decay.

Time-variable quantities:

Total activity— A, is the number of decays per unit time of a radioactive sample.

Number of particles—N, is the total number of particles in the sample.

Specific activity—S_A, number of decays per unit time per amount of substance of the sample at time set to zero (t = 0). "Amount of substance" can be the mass, volume or moles of the initial sampl

These are related as follows:

\( t_{1/2} = \frac{\ln(2)}{\lambda} = \tau \ln(2) \)
\( A = - \frac{\mathrm{d}N}{\mathrm{d}t} = \lambda N \)
\( S_A a_0 = - \frac{\mathrm{d}N}{\mathrm{d}t}\bigg|_{t=0} = \lambda N_0 \)

where N₀ is the initial amount of active substance — substance that has the same percentage of unstable particles as when the substance was formed.

Mathematics of radioactive decay
For the mathematical details of exponential decay in general context, see exponential decay.
For related derivations with some further details, see half-life.
For the analogous mathematics in 1st order chemical reactions, see Consecutive reactions.

Universal law of radioactive decay

Radioactivity is one very frequently given example of exponential decay. The law describes the statistical behaviour of a large number of nuclides, rather than individual atoms. In the following formalism, the number of nuclides or the nuclide population N, is of course a discrete variable (a natural number)—but for any physical sample N is so large that it can be treated as a continuous variable. Differential calculus is needed to set up differential equations for the modelling the behaviour of the nuclear decay.

The mathematics of radioactive decay depend on a key assumption that a nucleus of a radionuclide has no "memory" or way of translating its history into its present behavior. 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. This constant probability may vary greatly between different types of nuclei, leading to the many different observed decay rates. However, whatever the probability is, it does not change. This is in marked contrast to complex objects which do show aging, such as automobiles and humans. These systems do have a chance of breakdown per unit of time, that increases from the moment they begin their existence.

One-decay process

Consider the case of a nuclide A that decays into another B by some process A → B (emission of other particles, like electron neutrinos ν
e and electrons e− as in beta decay, are irrelevant in what follows). The decay of an unstable nucleus is entirely random and it is impossible to predict when a particular atom will decay.[1] However, it is equally likely to decay at any instant in time. Therefore, given a sample of a particular radioisotope, the number of decay events −dN expected to occur in a small interval of time dt is proportional to the number of atoms present N, that is[16]

\( -\frac{\mathrm{d}N}{\mathrm{d}t} \propto N. \)

Particular radionuclides decay at different rates, so each has its own decay constant λ. The expected decay −dN/N is proportional to an increment of time, dt:

\( -\frac{\mathrm{d}N}{N} = \lambda \mathrm{d}t \)

The negative sign indicates that N decreases as time increases, as the decay events follow one after another. The solution to this first-order differential equation is the function:

\( N(t) = N_0\,e^{-{\lambda}t} = N_0\,e^{-t/ \tau}, \,\! \)

where N₀ is the value of N at time t = 0.^[16]

We have for all time t:

\( N_A + N_B = N_\mathrm{total} = N_{A0}, \)

where N_total is the constant number of particles throughout the decay process, which is clearly equal to the initial number of A nuclides since this is the initial substance..

If the number of non-decayed A nuclei is:

\( N_A = N_{A0}e^{-{\lambda}t} \,\! \)

then the number of nuclei of B, i.e. the number of decayed A nuclei, is

\( N_B = N_{A0} - N_A = N_{A0} - N_{A0}e^{-{\lambda}t} = N_{A0} \left ( 1 - e^{-{\lambda}t} \right ). \)

The number of decays observed over a given interval obeys Poisson statistics. If the average number of decays is <N>, the probability of a given number of decays N is[16]

\( P(N) = \frac{\langle N \rangle^N \exp(-\langle N\rangle)}{N!} . \)

Chain-decay processes

Chain of two decays

Now consider the case of a chain of two decays: one nuclide A decaying into another B by one process, then B decaying into another C by a second process, i.e. A → B → C. The previous equation cannot be applied to the decay chain, but can be generalized as follows. Since A decays into B, then B decays into C, the activity of A adds to the total number of B nuclides in the present sample, before those B nuclides decay and reduce the number of nuclides leading to the later sample. In other words, the number of second generation nuclei B increases as a result of the first generation nuclei decay of A, and decreases as a result of its own decay into the third generation nuclei C.[17] The sum of these two terms gives the law for a decay chain for two nuclides:

\( \frac{\mathrm{d}N_B}{\mathrm{d}t} = -\lambda_B N_B + \lambda_A N_A. \)

The rate of change of N_B, that is dN_B/dt, is related to the changes in the amounts of A and B, N_B can increase as B is produced from A and decrease as B produces C.

Re-writing using the previous results:

\( \frac{\mathrm{d}N_B}{\mathrm{d}t} = - \lambda_B N_B + \lambda_A N_{A0} e^{-\lambda_A t} \)

The subscripts simply refer to the respective nuclides, i.e. N_A is the number of nuclides of type A, N_A0 is the initial number of nuclides of type A, λ_A is the decay constant for A - and similarly for nuclide B. Solving this equation for N_B gives:

\( N_B = \frac{N_{A0}\lambda_A}{\lambda_B - \lambda_A} \left ( e^{-\lambda_A t} - e^{-\lambda_B t}\right ) . \)

Naturally, in the case where B is a stable nuclide (λB = 0), this equation reduces to the previous solution, in the case :

\( \lim_{\lambda_B\rightarrow 0} \left [ \frac{N_{A0}\lambda_A}{\lambda_B - \lambda_A} \left ( e^{-\lambda_A t} - e^{-\lambda_B t}\right ) \right ] = \frac{N_{A0}\lambda_A}{0 - \lambda_A} \left ( e^{-\lambda_A t} - 1 \right ) = N_{A0} \left ( 1- e^{-\lambda_A t} \right ), \)

as shown above for one decay. The solution can be found by the integration factor method, where the integrating factor is eλBt. This case is perhaps the most useful, since it can derive both the one-decay equation (above) and the equation for multi-decay chains (below) more directly.

Chain of any number of decays

For the general case of any number of consecutive decays in a decay chain, i.e. A₁ → A₂ ··· → A_i ··· → A_D, where D is the number of decays and i is a dummy index (i = _{1, 2, 3, ...D}), each nuclide population can be found in terms of the previous population. In this case N₂ = 0, N₃ = 0,..., N_D = 0. Using the above result in a recursive form:

\( \frac{\mathrm{d}N_j}{\mathrm{d}t} = - \lambda_j N_j + \lambda_{j-1} N_{(j-1)0} e^{-\lambda_{j-1} t}. \)

The general solution to the recursive problem is given by Bateman's equations:[18]

Bateman's equations

\( N_D = \frac{N_1(0)}{\lambda_D} \sum_{i=1}^D \lambda_i c_i e^{-\lambda_i t} \)

\( c_i = \prod_{j=1, i\neq j}^D \frac{\lambda_j}{\lambda_j - \lambda_i} \)

Alternative decay modes

In all of the above examples, the initial nuclide decays into only one product.[19] Consider the case of one initial nuclide that can decay into either of two products, that is A → B and A → C in parallel. For example, in a sample of potassium-40, 89.3% of the nuclei decay to calcium-40 and 10.7% to argon-40. We have for all time t:

\( N = N_A + N_B + N_C \)

which is constant, since the total number of nuclides remains constant. Differentiating with respect to time:

\( \begin{align} \frac{\mathrm{d}N_A}{\mathrm{d}t} & = - \left(\frac{\mathrm{d}N_B}{\mathrm{d}t} + \frac{\mathrm{d}N_C}{\mathrm{d}t} \right) \\ - \lambda N_A & = - N_A \left ( \lambda_B + \lambda_C \right ) \\ \end{align} \)

defining the total decay constant λ in terms of the sum of partial decay constants λB and λC:

\( \lambda = \lambda_B + \lambda_C . \)

Notice that

\( \frac{\mathrm{d}N_A}{\mathrm{d}t} < 0,\frac{\mathrm{d}N_B}{\mathrm{d}t} > 0, \frac{\mathrm{d}N_C}{\mathrm{d}t} > 0.

Solving this equation for NA:

\( N_A = N_{A0} e^{-\lambda t} . \)

where N_A0 is the initial number of nuclide A. When measuring the production of one nuclide, one can only observe the total decay constant λ. The decay constants λ_B and λ_C determine the probability for the decay to result in products B or C as follows:

\( N_B = \frac{\lambda_B}{\lambda} N_{A0} \left ( 1 - e^{-\lambda t} \right ), \)

\( N_C = \frac{\lambda_C}{\lambda} N_{A0} \left ( 1 - e^{-\lambda t} \right ). \)

because the fraction λB/λ of nuclei decay into B while the fraction λC/λ of nuclei decay into C.
Corollaries of the decay laws

The above equations can also be written using quantities related to the number of nuclide particles N in a sample;

The activity: A = λN.
The amount of substance: n = N/L.
The mass: M = Arn = ArN/L.

where L = 6.022×10²³ is Avogadro's constant, A_r is the relative atomic mass number, and the amount of the substance is in moles.

Decay timing: definitions and relations
Time constant and mean-life

For the one-decay solution A → B:

\( N = N_0\,e^{-{\lambda}t} = N_0\,e^{-t/ \tau}, \,\! \)

the equation indicates that the decay constant λ has units of t−1, and can thus also be represented as 1/τ, where τ is a characteristic time of the process called the time constant.

In a radioactive decay process, this time constant is also the mean lifetime for decaying atoms. Each atom "lives" for a finite amount of time before it decays, and it may be shown that this mean lifetime is the arithmetic mean of all the atoms' lifetimes, and that it is τ, which again is related to the decay constant as follows:

\( \tau = \frac{1}{\lambda}. \)

This form is also true for two-decay processes simultaneously A → B + C, inserting the equivalent values of decay constants (as given above)

\( \lambda = \lambda_B + \lambda_C \, \)

into the decay solution leads to:

\( \frac{1}{\tau} = \lambda = \lambda_B + \lambda_C = \frac{1}{\tau_B} + \frac{1}{\tau_C}\, \)

Simulation of many identical atoms undergoing radioactive decay, starting with either 4 atoms (left) or 400 (right). The number at the top indicates how many half-lives have elapsed. Note the law of large numbers: with more atoms, the overall decay is less random.

Half-life

A more commonly used parameter is the half-life. Given a sample of a particular radionuclide, the half-life is the time taken for half the radionuclide's atoms to decay. For the case of one-decay nuclear reactions:

\( N = N_0\,e^{-{\lambda}t} = N_0\,e^{-t/ \tau}, \,\! \)

the half-life is related to the decay constant as follows: set N = N0/2 and t = T1/2 to obtain

\( t_{1/2} = \frac{\ln 2}{\lambda} = \tau \ln 2. \)

This relationship between the half-life and the decay constant shows that highly radioactive substances are quickly spent, while those that radiate weakly endure longer. Half-lives of known radionuclides vary widely, from more than 1019 years, such as for the very nearly stable nuclide 209Bi, to 10⁻²³ seconds for highly unstable ones.

The factor of ln(2) in the above relations results from the fact that concept of "half-life" is merely a way of selecting a different base other than the natural base e for the lifetime expression. The time constant τ is the e -1 -life, the time until only 1/e remains, about 36.8%, rather than the 50% in the half-life of a radionuclide. Thus, τ is longer than t1/2. The following equation can be shown to be valid:

\( N(t) = N_0\,e^{-t/ \tau} =N_0\,2^{-t/t_{1/2}}. \,\! \)

Since radioactive decay is exponential with a constant probability, each process could as easily be described with a different constant time period that (for example) gave its "(1/3)-life" (how long until only 1/3 is left) or "(1/10)-life" (a time period until only 10% is left), and so on. Thus, the choice of τ and t1/2 for marker-times, are only for convenience, and from convention. They reflect a fundamental principle only in so much as they show that the same proportion of a given radioactive substance will decay, during any time-period that one chooses.

Mathematically, the nth life for the above situation would be found in the same way as above—by setting N = N0/n, {{{1}}} and substituting into the decay solution to obtain

\( t_{1/n} = \frac{\ln n}{\lambda} = \tau \ln n. \)

Example

A sample of 14C has a half-life of 5,730 years and a decay rate of 14 disintegration per minute (dpm) per gram of natural carbon.

If an artifact is found to have radioactivity of 4 dpm per gram of its present C, we can find the approximate age of the object using the above equation:

\( N = N_0\,e^{-t/ \tau}, \)

where: \(\frac{N}{ N_0} = 4/14 \approx 0.286, \)

\( \tau = \frac{T_{1/2}}{\ln 2} \approx 8267 \) years,
\( t = -\tau\,\ln\frac{N}{ N_0} \approx 10360 \) years.

Changing decay rates

The radioactive decay modes of electron capture and internal conversion are known to be slightly sensitive to chemical and environmental effects that change the electronic structure of the atom, which in turn affects the presence of 1s and 2s electrons that participate in the decay process. A small number of mostly light nuclides are affected. For example, chemical bonds can affect the rate of electron capture to a small degree (in general, less than 1%) depending on the proximity of electrons to the nucleus. In 7Be, a difference of 0.9% has been observed between half-lives in metallic and insulating environments.[20] This relatively large effect is because beryllium is a small atom whose valence electrons are in 2s atomic orbitals, which are subject to electron capture in 7Be because (like all s atomic orbitals in all atoms) they naturally penetrate into the nucleus.

In 1992, Jung et al. of the Darmstadt Heavy-Ion Research group observed an accelerated β decay of 163Dy66+. Although neutral 163Dy is a stable isotope, the fully ionized 163Dy66+ undergoes β decay into the K and L shells with a half-life of 47 days.[21]

Rhenium-187 is another spectacular example. 187Re normally beta decays to 187Os with a half-life of 41.6 × 109 years,[22] but studies using fully ionised 187Re atoms (bare nuclei) have found that this can decrease to only 33 years. This is attributed to "bound-state β− decay" of the fully ionised atom – the electron is emitted into the "K-shell" (1s atomic orbital), which cannot occur for neutral atoms in which all low-lying bound states are occupied.[23]
Decay Rate of Radon-222 as a function of date and time of day. The color-bar gives the power of the observed signal and represents ~4% seasonal decay rate variation.

A number of experiments have found that decay rates of other modes of artificial and naturally occurring radioisotopes are, to a high degree of precision, unaffected by external conditions such as temperature, pressure, the chemical environment, and electric, magnetic, or gravitational fields.[24] Comparison of laboratory experiments over the last century, studies of the Oklo natural nuclear reactor (which exemplified the effects of thermal neutrons on nuclear decay), and astrophysical observations of the luminosity decays of distant supernovae (which occurred far away so the light has taken a great deal of time to reach us), for example, strongly indicate that unperturbed decay rates have been constant (at least to within the limitations of small experimental errors) as a function of time as well.[citation needed]

Recent results suggest the possibility that decay rates might have a weak dependence on environmental factors. It has been suggested that measurements of decay rates of silicon-32, manganese-54, and radium-226 exhibit small seasonal variations (of the order of 0.1%),[25][26][27] while the decay of Radon-222 exhibit large 4% peak-to-peak seasonal variations,[28] proposed to be related to either solar flare activity or distance from the Sun. However, such measurements are highly susceptible to systematic errors, and a subsequent paper[29] has found no evidence for such correlations in seven other isotopes (22Na, 44Ti, 108Ag, 121Sn, 133Ba, 241Am, 238Pu), and sets upper limits on the size of any such effects.
Theoretical basis of decay phenomena
This section possibly contains original research. Please improve it by verifying the claims made and adding inline citations. Statements consisting only of original research should be removed. (October 2014)

The neutrons and protons that constitute nuclei, as well as other particles that approach close enough to them, are governed by several interactions. The strong nuclear force, not observed at the familiar macroscopic scale, is the most powerful force over subatomic distances. The electrostatic force is almost always significant, and, in the case of beta decay, the weak nuclear force is also involved.

The interplay of these forces produces a number of different phenomena in which energy may be released by rearrangement of particles in the nucleus, or else the change of one type of particle into others. These rearrangements and transformations may be hindered energetically, so that they do not occur immediately. In certain cases, random quantum vacuum fluctuations are theorized to promote relaxation to a lower energy state (the "decay") in a phenomenon known as quantum tunneling. Radioactive decay half-life of nuclides has been measured over timescales of 55 orders of magnitude, from 2.3 x 10⁻²³ seconds (for hydrogen-7) to 6.9 x 10³¹ seconds (for tellurium-128).[30] The limits of these timescales are set by the sensitivity of instrumentation only, and there are no known natural limits to how brief or long a decay half life for radioactive decay of a radionuclide may be.

The decay process, like all hindered energy transformations, may be analogized by a snowfield on a mountain. While friction between the ice crystals may be supporting the snow's weight, the system is inherently unstable with regard to a state of lower potential energy. A disturbance would thus facilitate the path to a state of greater entropy: The system will move towards the ground state, producing heat, and the total energy will be distributable over a larger number of quantum states. Thus, an avalanche results. The total energy does not change in this process, but, because of the second law of thermodynamics, avalanches have only been observed in one direction and that is toward the "ground state" — the state with the largest number of ways in which the available energy could be distributed.

Such a collapse (a decay event) requires a specific activation energy. For a snow avalanche, this energy comes as a disturbance from outside the system, although such disturbances can be arbitrarily small. In the case of an excited atomic nucleus, the arbitrarily small disturbance comes from quantum vacuum fluctuations. A radioactive nucleus (or any excited system in quantum mechanics) is unstable, and can, thus, spontaneously stabilize to a less-excited system. The resulting transformation alters the structure of the nucleus and results in the emission of either a photon or a high-velocity particle that has mass (such as an electron, alpha particle, or other type).

Occurrence and applications

According to the Big Bang theory, stable isotopes of the lightest five elements (H, He, and traces of Li, Be, and B) were produced very shortly after the emergence of the universe, in a process called Big Bang nucleosynthesis. These lightest stable nuclides (including deuterium) survive to today, but any radioactive isotopes of the light elements produced in the Big Bang (such as tritium) have long since decayed. Isotopes of elements heavier than boron were not produced at all in the Big Bang, and these first five elements do not have any long-lived radioisotopes. Thus, all radioactive nuclei are, therefore, relatively young with respect to the birth of the universe, having formed later in various other types of nucleosynthesis in stars (in particular, supernovae), and also during ongoing interactions between stable isotopes and energetic particles. For example, carbon-14, a radioactive nuclide with a half-life of only 5,730 years, is constantly produced in Earth's upper atmosphere due to interactions between cosmic rays and nitrogen.

Nuclides that are produced by radioactive decay are called radiogenic nuclides, whether they themselves are stable or not. There exist stable radiogenic nuclides that were formed from short-lived extinct radionuclides in the early solar system.[31][32] The extra presence of these stable radiogenic nuclides (such as Xe-129 from primordial I-129) against the background of primordial stable nuclides can be inferred by various means.

Radioactive decay has been put to use in the technique of radioisotopic labeling, which is used to track the passage of a chemical substance through a complex system (such as a living organism). A sample of the substance is synthesized with a high concentration of unstable atoms. The presence of the substance in one or another part of the system is determined by detecting the locations of decay events.

On the premise that radioactive decay is truly random (rather than merely chaotic), it has been used in hardware random-number generators. Because the process is not thought to vary significantly in mechanism over time, it is also a valuable tool in estimating the absolute ages of certain materials. For geological materials, the radioisotopes and some of their decay products become trapped when a rock solidifies, and can then later be used (subject to many well-known qualifications) to estimate the date of the solidification. These include checking the results of several simultaneous processes and their products against each other, within the same sample. In a similar fashion, and also subject to qualification, the rate of formation of carbon-14 in various eras, the date of formation of organic matter within a certain period related to the isotope's half-life may be estimated, because the carbon-14 becomes trapped when the organic matter grows and incorporates the new carbon-14 from the air. Thereafter, the amount of carbon-14 in organic matter decreases according to decay processes that may also be independently cross-checked by other means (such as checking the carbon-14 in individual tree rings, for example).

Origins of radioactive nuclides
Main article: nucleosynthesis

Radioactive primordial nuclides found in the Earth are residues from ancient supernova explosions which occurred before the formation of the solar system. They are the long-lived fraction of radionuclides surviving in the primordial solar nebula through planet accretion until the present. The naturally occurring short-lived radiogenic radionuclides found in rocks are the daughters of these radioactive primordial nuclides. Another minor source of naturally occurring radioactive nuclides are cosmogenic nuclides, formed by cosmic ray bombardment of material in the Earth's atmosphere or crust. The radioactive decay of these radionuclides in rocks within Earth's mantle and crust contribute significantly to Earth's internal heat budget.
Decay chains and multiple modes

The daughter nuclide of a decay event may also be unstable (radioactive). In this case, it will also decay, producing radiation. The resulting second daughter nuclide may also be radioactive. This can lead to a sequence of several decay events. Eventually, a stable nuclide is produced. This is called a decay chain (see this article for specific details of important natural decay chains).
Gamma-ray energy spectrum of uranium ore (inset). Gamma-rays are emitted by decaying nuclides, and the gamma-ray energy can be used to characterize the decay (which nuclide is decaying to which). Here, using the gamma-ray spectrum, several nuclides that are typical of the decay chain of 238U have been identified: 226Ra, 214Pb, 214Bi.

An example is the natural decay chain of 238U, which is as follows:

decays, through alpha-emission, with a half-life of 4.5 billion years to thorium-234
which decays, through beta-emission, with a half-life of 24 days to protactinium-234
which decays, through beta-emission, with a half-life of 1.2 minutes to uranium-234
which decays, through alpha-emission, with a half-life of 240 thousand years to thorium-230
which decays, through alpha-emission, with a half-life of 77 thousand years to radium-226
which decays, through alpha-emission, with a half-life of 1.6 thousand years to radon-222
which decays, through alpha-emission, with a half-life of 3.8 days to polonium-218
which decays, through alpha-emission, with a half-life of 3.1 minutes to lead-214
which decays, through beta-emission, with a half-life of 27 minutes to bismuth-214
which decays, through beta-emission, with a half-life of 20 minutes to polonium-214
which decays, through alpha-emission, with a half-life of 160 microseconds to lead-210
which decays, through beta-emission, with a half-life of 22 years to bismuth-210
which decays, through beta-emission, with a half-life of 5 days to polonium-210
which decays, through alpha-emission, with a half-life of 140 days to lead-206, which is a stable nuclide.

Some radionuclides may have several different paths of decay. For example, approximately 36% of bismuth-212 decays, through alpha-emission, to thallium-208 while approximately 64% of bismuth-212 decays, through beta-emission, to polonium-212. Both thallium-208 and polonium-212 are radioactive daughter products of bismuth-212, and both decay directly to stable lead-208.
Associated hazard warning signs

The trefoil symbol used to indicate ionising radiation.

2007 ISO radioactivity danger symbol intended for IAEA Category 1, 2 and 3 sources defined as dangerous sources capable of death or serious injury.[33]

The dangerous goods transport classification sign for radioactive materials

See also
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Actinides in the environment
Background radiation
Chernobyl disaster
Crimes involving radioactive substances
Decay chain
Fallout shelter
Half-life
Lists of nuclear disasters and radioactive incidents
National Council on Radiation Protection and Measurements
Nuclear engineering
Nuclear medicine
Nuclear pharmacy
Nuclear physics
Nuclear power
Particle decay
Poisson process
Radiation
Radiation therapy
Radioactive contamination
Radioactivity in biology
Radiometric dating
Radionuclide a.k.a. "radio-isotope"
Secular equilibrium
Transient equilibrium

Notes

Radionuclide is the more correct term, but radioisotope is also used. The difference between isotope and nuclide is explained at Isotope#Isotope vs. nuclide.

References
Inline

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IAEA news release Feb 2007

General

"Radioactivity", Encyclopædia Britannica. 2006. Encyclopædia Britannica Online. December 18, 2006
Radio-activity by Ernest Rutherford Phd, Encyclopædia Britannica Eleventh Edition

External links
Look up radioactivity in Wiktionary, the free dictionary.

The Lund/LBNL Nuclear Data Search – Contains tabulated information on radioactive decay types and energies.
Nomenclature of nuclear chemistry
Specific activity and related topics.
The Live Chart of Nuclides – IAEA
Health Physics Society Public Education Website
Wikisource-logo.svg Beach, Chandler B., ed. (1914). "Becquerel Rays". The New Student's Reference Work. Chicago: F. E. Compton and Co.
Annotated bibliography for radioactivity from the Alsos Digital Library for Nuclear Issues
Stochastic Java applet on the decay of radioactive atoms by Wolfgang Bauer
Stochastic Flash simulation on the decay of radioactive atoms by David M. Harrison
"Henri Becquerel: The Discovery of Radioactivity", Becquerel's 1896 articles online and analyzed on BibNum [click 'à télécharger' for English version].
"Radioactive change", Rutherford & Soddy article (1903), online and analyzed on Bibnum [click 'à télécharger' for English version].

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