300px|thumb|A possible [[nuclear fission chain reaction: <br/>

1) A uranium-235 atom absorbs a neutron and fissions into two fission fragments, releasing three new neutrons and a large amount of binding energy. <br/>

2) One of those neutrons is absorbed by an atom of uranium-238, and does not continue the reaction. Another neutron leaves the system without being absorbed. However, one neutron does collide with an atom of uranium-235, which then fissions and releases two neutrons and more binding energy. <br/>

3) Both of those neutrons collide with uranium-235 atoms, each of which fissions and releases a few neutrons, which can then continue the reaction.]]

In nuclear physics, a nuclear chain reaction occurs when one single nuclear reaction causes an average of one or more subsequent nuclear reactions, thus leading to the possibility of a self-propagating series or "positive feedback loop" of these reactions. The specific nuclear reaction may be the fission of heavy isotopes (e.g., uranium-235, <sup>235</sup>U). A nuclear chain reaction releases several million times more energy per reaction than any chemical reaction.

History

Chemical chain reactions were first proposed by German chemist Max Bodenstein in 1913, and were reasonably well understood before nuclear chain reactions were proposed. It was understood that chemical chain reactions were responsible for exponentially increasing rates in reactions, such as produced in chemical explosions.

The concept of a nuclear chain reaction was reportedly first hypothesized by Hungarian scientist Leó Szilárd on September 12, 1933. Szilárd that morning had been reading in a London paper of an experiment in which protons from an accelerator had been used to split lithium-7 into alpha particles, and the fact that much greater amounts of energy were produced by the reaction than the proton supplied. Ernest Rutherford commented in the article that inefficiencies in the process precluded use of it for power generation. However, the neutron had been discovered by James Chadwick in 1932, shortly before, as the product of a nuclear reaction. Szilárd, who had been trained as an engineer and physicist, put the two nuclear experimental results together in his mind and realized that if a nuclear reaction produced neutrons, which then caused further similar nuclear reactions, the process might be a self-perpetuating nuclear chain reaction, spontaneously producing new isotopes and power without the need for protons or an accelerator. Szilárd, however, did not propose fission as the mechanism for his chain reaction since the fission reaction was not yet discovered, or even suspected. Instead, Szilárd proposed using mixtures of lighter known isotopes which produced neutrons in copious amounts. He filed a patent for his idea of a simple nuclear reactor the following year.

In 1936, Szilárd attempted to create a chain reaction using beryllium and indium but was unsuccessful. Nuclear fission was discovered by Otto Hahn and Fritz Strassmann in December 1938 and explained theoretically in January 1939 by Lise Meitner and her nephew Otto Robert Frisch. In their second publication on nuclear fission in February 1939, Hahn and Strassmann used the term Uranspaltung (uranium fission) for the first time and predicted the existence and liberation of additional neutrons during the fission process, opening up the possibility of a nuclear chain reaction.

A few months later, Frédéric Joliot-Curie, H. Von Halban and L. Kowarski in Paris searched for, and discovered, neutron multiplication in uranium, proving that a nuclear chain reaction by this mechanism was indeed possible. On May 4, 1939, Joliot-Curie, Halban, and Kowarski filed three patents. The first two described power production from a nuclear chain reaction, the last one called Perfectionnement aux charges explosives was the first patent for the atomic bomb and is filed as patent No. 445686 by the Caisse nationale de Recherche Scientifique. In parallel, Szilárd and Enrico Fermi in New York made the same analysis. This discovery prompted the letter from Szilárd and signed by Albert Einstein to President Franklin D. Roosevelt, warning of the possibility that Nazi Germany might be attempting to build an atomic bomb.

In 1942, Gertrude Scharff Goldhaber demonstrates that uranium under spontaneous fission produces multiple neutrons, with energy sufficient for a chain reaction. On December 2, 1942, a team led by Fermi (and including Szilárd) produced the first artificial self-sustaining nuclear chain reaction with the Chicago Pile-1 experimental reactor in a racquets court below the bleachers of Stagg Field at the University of Chicago. Fermi's experiments at the University of Chicago were part of Arthur H. Compton's Metallurgical Laboratory of the Manhattan Project; the lab was renamed Argonne National Laboratory and tasked with conducting research in harnessing fission for nuclear energy.

In 1956, Paul Kuroda of the University of Arkansas postulated that a natural fission reactor may have once existed. Since nuclear chain reactions may only require natural materials (such as water and uranium, if the uranium has sufficient amounts of <sup>235</sup>U), it was possible to have these chain reactions occur in the distant past when uranium-235 concentrations were higher than today, and where there was the right combination of materials within the Earth's crust. Uranium-235 made up a larger share of uranium on Earth in the geological past because of the different half-lives of the isotopes and , the former decaying almost an order of magnitude faster than the latter. Kuroda's prediction was verified with the discovery of evidence of natural self-sustaining nuclear chain reactions in the past at Oklo in Gabon in September 1972. To sustain a nuclear fission chain reaction at present isotope ratios in natural uranium on Earth would require the presence of a neutron moderator like heavy water or high purity carbon (e.g. graphite) in the absence of neutron poisons, which is even more unlikely to arise by natural geological processes than the conditions at Oklo some two billion years ago.

Process

Fission chain reactions occur because of interactions between neutrons and fissile isotopes (such as <sup>235</sup>U). The chain reaction requires both the release of neutrons from fissile isotopes undergoing nuclear fission and the subsequent absorption of some of these neutrons in fissile isotopes. When an atom undergoes nuclear fission, a few neutrons (the exact number depends on uncontrollable and unmeasurable factors; the expected number depends on several factors, usually between 2.5 and 3.0) are ejected from the reaction. These free neutrons will then interact with the surrounding medium, and if more fissile fuel is present, some may be absorbed and cause more fissions. Thus, the cycle repeats to produce a reaction that is self-sustaining.

Nuclear power plants operate by precisely controlling the rate at which nuclear reactions occur. Nuclear weapons, on the other hand, are specifically engineered to produce a reaction that is so fast and intense it cannot be controlled after it has started. When properly designed, this uncontrolled reaction will lead to an explosive energy release.

Fuel

Nuclear weapons employ high quality, highly enriched fuel exceeding the critical size and geometry (critical mass) necessary in order to obtain an explosive chain reaction. The fuel for energy purposes, such as in a nuclear fission reactor, is very different, usually consisting of a low-enriched oxide material (e.g. uranium dioxide, UO<sub>2</sub>). There are two primary isotopes used for fission reactions inside of nuclear reactors.

The first and most common is uranium-235. This is the fissile isotope of uranium and it makes up approximately 0.7% of all naturally occurring uranium. Because of the small amount of <sup>235</sup>U that exists, it is considered a non-renewable energy source despite being found in rock formations around the world. Uranium-235 cannot be used as fuel in its base form for energy production; it must undergo a process known as refinement to produce the compound UO<sub>2</sub>. The UO<sub>2</sub> is then pressed and formed into ceramic pellets, which can subsequently be placed into fuel rods. This is when UO<sub>2</sub> can be used for nuclear power production.

The second most common isotope used in nuclear fission is plutonium-239, because it is able to become fissile with slow neutron interaction. This isotope is formed inside nuclear reactors by exposing <sup>238</sup>U to the neutrons released during fission. As a result of neutron capture, uranium-239 is produced, which undergoes two beta decays to become plutonium-239. Plutonium once occurred as a primordial element in Earth's crust, but only trace amounts remain so it is predominantly synthetic.

Another proposed fuel for nuclear reactors, which however plays no commercial role as of 2021, is uranium-233, which is "bred" by neutron capture and subsequent beta decays from natural thorium, which is almost 100% composed of the isotope thorium-232. This is called the thorium fuel cycle.

Enrichment process

The fissile isotope uranium-235 in its natural concentration is unfit for the vast majority of nuclear reactors. In order to be prepared for use as fuel in energy production, it must be enriched. The enrichment process does not apply to plutonium. Reactor-grade plutonium is created as a byproduct of neutron interaction between two different isotopes of uranium.

The first step to enriching uranium begins by converting uranium oxide (created through the uranium milling process) into a gaseous form. This gas is known as uranium hexafluoride, which is created by combining hydrogen fluoride, fluorine, and uranium oxide. Uranium dioxide is also present in this process and is sent off to be used in reactors not requiring enriched fuel. The remaining uranium hexafluoride compound is drained into metal cylinders where it solidifies. The next step is separating the uranium hexafluoride from the depleted U-235 left over. This is typically done with centrifuges that spin fast enough to allow for the 1% mass difference in uranium isotopes to separate themselves. A laser is then used to enrich the hexafluoride compound. The final step involves reconverting the enriched compound back into uranium oxide, leaving the final product: enriched uranium oxide. This form of UO<sub>2</sub> can now be used in fission reactors inside power plants to produce energy.

Reaction products

When a fissile atom undergoes nuclear fission, it breaks into two or more fission fragments. Also, several free neutrons, gamma rays, and neutrinos are emitted, and a large amount of energy is released. The sum of the rest masses of the fission fragments and ejected neutrons is less than the sum of the rest masses of the original atom and incident neutron (of course the fission fragments are not at rest). The mass difference is accounted for in the release of energy according to the equation E=Δmc<sup>2</sup>:

:mass of released energy = <math>\frac{E}{c^2} = m_\text{original}-m_\text{final}</math>

Due to the extremely large value of the speed of light, c, a small decrease in mass is associated with a tremendous release of active energy (for example, the kinetic energy of the fission fragments). This energy (in the form of radiation and heat) carries the missing mass when it leaves the reaction system (total mass, like total energy, is always conserved). While typical chemical reactions release energies on the order of a few eVs (e.g. the binding energy of the electron to hydrogen is 13.6&nbsp;eV), nuclear fission reactions typically release energies on the order of hundreds of millions of eVs.

Two typical fission reactions are shown below with average values of energy released and number of neutrons ejected:

:<math chem>\begin{align}

\ce{^{235}U + neutron ->} &\ \text{fission fragments} + 2.4\text{ neutrons} + 192.9\text{ MeV} \\

\ce{^{239}Pu + neutron ->} &\ \text{fission fragments} + 2.9\text{ neutrons} + 198.5\text{ MeV}

\end{align}</math>

Note that these equations are for fissions caused by slow-moving (thermal) neutrons. The average energy released and number of neutrons ejected is a function of the incident neutron speed.

Mean generation time

The mean generation time, <math>\Lambda</math>, is the average time from a neutron emission to a capture that results in fission.

To keep the probability of predetonation low, the duration of the non-optimal assembly period is minimized, and fissile and other materials are used that have low spontaneous fission rates. In fact, the combination of materials has to be such that it is unlikely that there is even a single spontaneous fission during the period of supercritical assembly. In particular, the gun method cannot be used with plutonium.

Nuclear power plants and control of chain reactions

Chain reactions naturally give rise to reaction rates that grow (or shrink) exponentially, whereas a nuclear power reactor needs to be able to hold the reaction rate reasonably constant. To maintain this control, the chain reaction criticality must have a slow enough time scale to permit intervention by additional effects, such as via mechanical control rods or thermal expansion. Consequently, all nuclear power reactors (even fast-neutron reactors) rely on delayed neutrons for their criticality. An operating nuclear power reactor fluctuates between being slightly subcritical and slightly delayed-supercritical, but must always remain below prompt-critical.

It is impossible for a nuclear power plant to undergo a nuclear chain reaction that results in an explosion of power comparable with a nuclear weapon, but even low-powered explosions from uncontrolled chain reactions (that would be considered "fizzles" in a bomb) may still cause considerable damage and meltdown in a reactor. For example, the Chernobyl disaster involved a runaway chain reaction, but the result was a low-powered steam explosion from the relatively small release of heat, as compared with a bomb. However, the reactor complex was destroyed by the generated heat, as well as by ordinary burning of the graphite exposed to air. Such steam explosions would be typical of the very diffuse assembly of materials in a nuclear reactor, even under the worst conditions.

Other steps can be taken to boost safety as well. For example, power plants licensed in the United States require a negative void coefficient of reactivity: if coolant were to be removed from the reactor core, the nuclear reaction must tend toward shutting down, not toward increasing. This eliminates the possibility of the type of accident that occurred at Chernobyl (which was caused by a positive void coefficient). However, nuclear reactors are still capable of causing smaller chemical explosions even after complete shutdown, such as was the case with the Fukushima Daiichi nuclear disaster. In such cases, residual decay heat from the core may cause high temperatures if there is loss of coolant flow, even a day after the chain reaction has been shut down . This may cause a chemical reaction between water and fuel that produces hydrogen gas, which can explode after mixing with air, with severe contamination consequences, since fuel rod material may still be exposed to the atmosphere from this process. However, such explosions do not happen during a chain reaction, but rather as a result of energy from radioactive beta decay, after the fission chain reaction has been stopped.

See also

  • Proton–proton chain
  • Criticality accident
  • Nuclear physics

References

  • Nuclear Chain Reaction Animation
  • Annotated bibliography on nuclear chain reactions from the Alsos Digital Library
  • Stochastic Java simulation of nuclear chain reaction by Wolfgang Bauer