Neutron capture

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Neutron capture is a nuclear reaction in which an atomic nucleus and one or more neutrons collide and merge to form a heavier nucleus. [1] Since neutrons have no electric charge, they can enter a nucleus more easily than positively charged protons, which are repelled electrostatically. [1]

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Neutron capture plays a significant role in the cosmic nucleosynthesis of heavy elements. In stars it can proceed in two ways: as a rapid process (r-process) or a slow process (s-process). [1] Nuclei of masses greater than 56 cannot be formed by thermonuclear reactions (i.e., by nuclear fusion) but can be formed by neutron capture. [1] Neutron capture on protons yields a line at 2.223 MeV predicted [2] and commonly observed [3] in solar flares.

Neutron capture at small neutron flux

Decay scheme of Au Au-198 Decay Scheme.svg
Decay scheme of Au

At small neutron flux, as in a nuclear reactor, a single neutron is captured by a nucleus. For example, when natural gold (197Au) is irradiated by neutrons (n), the isotope 198Au is formed in a highly excited state, and quickly decays to the ground state of 198Au by the emission of gamma rays (𝛾). In this process, the mass number increases by one. This is written as a formula in the form 197Au + n → 198Au + γ, or in short form 197Au(n,γ)198Au. If thermal neutrons are used, the process is called thermal capture.

The isotope 198Au is a beta emitter that decays into the mercury isotope 198Hg. In this process, the atomic number rises by one.

Neutron capture at high neutron flux

The r-process happens inside stars if the neutron flux density is so high that the atomic nucleus has no time to decay via beta emission between neutron captures. The mass number therefore rises by a large amount while the atomic number (i.e., the element) stays the same. When further neutron capture is no longer possible, the highly unstable nuclei decay via many β decays to beta-stable isotopes of higher-numbered elements.

Capture cross section

The absorption neutron cross section of an isotope of a chemical element is the effective cross-sectional area that an atom of that isotope presents to absorption and is a measure of the probability of neutron capture. It is usually measured in barns.

Absorption cross section is often highly dependent on neutron energy. In general, the likelihood of absorption is proportional to the time the neutron is in the vicinity of the nucleus. The time spent in the vicinity of the nucleus is inversely proportional to the relative velocity between the neutron and nucleus. Other more specific issues modify this general principle. Two of the most specified measures are the cross section for thermal neutron absorption and the resonance integral, which considers the contribution of absorption peaks at certain neutron energies specific to a particular nuclide, usually above the thermal range, but encountered as neutron moderation slows the neutron from an original high energy.

The thermal energy of the nucleus also has an effect; as temperatures rise, Doppler broadening increases the chance of catching a resonance peak. In particular, the increase in uranium-238's ability to absorb neutrons at higher temperatures (and to do so without fissioning) is a negative feedback mechanism that helps keep nuclear reactors under control.

Thermochemical significance

Neutron capture is involved in the formation of isotopes of chemical elements. The energy of neutron capture thus intervenes[ clarification needed ] in the standard enthalpy of formation of isotopes.

Uses

Neutron activation analysis can be used to remotely detect the chemical composition of materials. This is because different elements release different characteristic radiation when they absorb neutrons. This makes it useful in many fields related to mineral exploration and security.

Neutron absorbers

Neutron cross section of boron (top curve is for B and bottom curve for B) Neutroncrosssectionboron.png
Neutron cross section of boron (top curve is for B and bottom curve for B)

In engineering, the most important neutron absorber is 10 B, used as boron carbide in nuclear reactor control rods or as boric acid as a coolant water additive in pressurized water reactors. Other neutron absorbers used in nuclear reactors are xenon, cadmium, hafnium, gadolinium, cobalt, samarium, titanium, dysprosium, erbium, europium, molybdenum and ytterbium. [4] All of these occur in nature as mixtures of various isotopes, some of which are excellent neutron absorbers. They may occur in compounds such as molybdenum boride, hafnium diboride, titanium diboride, dysprosium titanate and gadolinium titanate.

Hafnium absorbs neutrons avidly and it can be used in reactor control rods. However, it is found in the same ores as zirconium, which shares the same outer electron shell configuration and thus has similar chemical properties. Their nuclear properties are profoundly different: hafnium absorbs neutrons 600 times better than zirconium. The latter, being essentially transparent to neutrons, is prized for internal reactor parts, including the metallic cladding of the fuel rods. To use these elements in their respective applications, the zirconium must be separated from the naturally co-occurring hafnium. This can be accomplished economically with ion-exchange resins. [5]

See also

Related Research Articles

<span class="mw-page-title-main">Neutron</span> Subatomic particle with no charge

The neutron is a subatomic particle, symbol
n
or
n0
, which has a neutral charge, and a mass slightly greater than that of a proton. Protons and neutrons constitute the nuclei of atoms. Since protons and neutrons behave similarly within the nucleus, they are both referred to as nucleons. Nucleons have a mass of approximately one atomic mass unit, or dalton. Their properties and interactions are described by nuclear physics. Protons and neutrons are not elementary particles; each is composed of three quarks.

<span class="mw-page-title-main">Neutron activation analysis</span> Method used for determining the concentrations of elements in many materials

Neutron activation analysis (NAA) is a nuclear process used for determining the concentrations of elements in many materials. NAA allows discrete sampling of elements as it disregards the chemical form of a sample, and focuses solely on atomic nuclei. The method is based on neutron activation and thus requires a neutron source. The sample is bombarded with neutrons, causing its constituent elements to form radioactive isotopes. The radioactive emissions and radioactive decay paths for each element have long been studied and determined. Using this information, it is possible to study spectra of the emissions of the radioactive sample, and determine the concentrations of the various elements within it. A particular advantage of this technique is that it does not destroy the sample, and thus has been used for the analysis of works of art and historical artifacts. NAA can also be used to determine the activity of a radioactive sample.

<span class="mw-page-title-main">Nuclear fission</span> Nuclear reaction splitting an atom into multiple parts

Nuclear fission is a reaction in which the nucleus of an atom splits into two or more smaller nuclei. The fission process often produces gamma photons, and releases a very large amount of energy even by the energetic standards of radioactive decay.

<span class="mw-page-title-main">Beta particle</span> Ionizing radiation

A beta particle, also called beta ray or beta radiation, is a high-energy, high-speed electron or positron emitted by the radioactive decay of an atomic nucleus during the process of beta decay. There are two forms of beta decay, β decay and β+ decay, which produce electrons and positrons respectively.

In nuclear engineering, fissile material is material that can undergo nuclear fission when struck by a neutron of low energy. A self-sustaining thermal chain reaction can only be achieved with fissile material. The predominant neutron energy in a system may be typified by either slow neutrons or fast neutrons. Fissile material can be used to fuel thermal-neutron reactors, fast-neutron reactors and nuclear explosives.

<span class="mw-page-title-main">Nuclear isomer</span> Metastable excited state of a nuclide

A nuclear isomer is a metastable state of an atomic nucleus, in which one or more nucleons (protons or neutrons) occupy excited state (higher energy) levels. "Metastable" describes nuclei whose excited states have half-lives 100 to 1000 times longer than the half-lives of the excited nuclear states that decay with a "prompt" half life (ordinarily on the order of 10−12 seconds). The term "metastable" is usually restricted to isomers with half-lives of 10−9 seconds or longer. Some references recommend 5 × 10−9 seconds to distinguish the metastable half life from the normal "prompt" gamma-emission half-life. Occasionally the half-lives are far longer than this and can last minutes, hours, or years. For example, the 180m
73
Ta
nuclear isomer survives so long (at least 1015 years) that it has never been observed to decay spontaneously. The half-life of a nuclear isomer can even exceed that of the ground state of the same nuclide, as shown by 180m
73
Ta
as well as 186m
75
Re
, 192m2
77
Ir
, 210m
83
Bi
, 212m
84
Po
, 242m
95
Am
and multiple holmium isomers.

<span class="mw-page-title-main">Neutron radiation</span> Ionizing radiation that presents as free neutrons

Neutron radiation is a form of ionizing radiation that presents as free neutrons. Typical phenomena are nuclear fission or nuclear fusion causing the release of free neutrons, which then react with nuclei of other atoms to form new nuclides—which, in turn, may trigger further neutron radiation. Free neutrons are unstable, decaying into a proton, an electron, plus an electron antineutrino. Free neutrons have a mean lifetime of 887 seconds.

<span class="mw-page-title-main">Nuclear reaction</span> Transformation of a nuclide to another

In nuclear physics and nuclear chemistry, a nuclear reaction is a process in which two nuclei, or a nucleus and an external subatomic particle, collide to produce one or more new nuclides. Thus, a nuclear reaction must cause a transformation of at least one nuclide to another. If a nucleus interacts with another nucleus or particle, they then separate without changing the nature of any nuclide, the process is simply referred to as a type of nuclear scattering, rather than a nuclear reaction.

<span class="mw-page-title-main">Control rod</span> Device used to regulate the power of a nuclear reactor

Control rods are used in nuclear reactors to control the rate of fission of the nuclear fuel – uranium or plutonium. Their compositions include chemical elements such as boron, cadmium, silver, hafnium, or indium, that are capable of absorbing many neutrons without themselves decaying. These elements have different neutron capture cross sections for neutrons of various energies. Boiling water reactors (BWR), pressurized water reactors (PWR), and heavy-water reactors (HWR) operate with thermal neutrons, while breeder reactors operate with fast neutrons. Each reactor design can use different control rod materials based on the energy spectrum of its neutrons. Control rods have been used in nuclear aircraft engines like Project Pluto as a method of control.

<span class="mw-page-title-main">Cowan–Reines neutrino experiment</span> Institute of Technology Experimental confirmation of neutrinos

The Cowan–Reines neutrino experiment was conducted by physicists Clyde Cowan and Frederick Reines in 1956. The experiment confirmed the existence of neutrinos. Neutrinos, subatomic particles with no electric charge and very small mass, had been conjectured to be an essential particle in beta decay processes in the 1930s. With neither mass nor charge, such particles appeared to be impossible to detect. The experiment exploited a huge flux of electron antineutrinos emanating from a nearby nuclear reactor and a detector consisting of large tanks of water. Neutrino interactions with the protons of the water were observed, verifying the existence and basic properties of this particle for the first time.

<span class="mw-page-title-main">Neutron activation</span> Induction of radioactivity by neutron radiation

Neutron activation is the process in which neutron radiation induces radioactivity in materials, and occurs when atomic nuclei capture free neutrons, becoming heavier and entering excited states. The excited nucleus decays immediately by emitting gamma rays, or particles such as beta particles, alpha particles, fission products, and neutrons. Thus, the process of neutron capture, even after any intermediate decay, often results in the formation of an unstable activation product. Such radioactive nuclei can exhibit half-lives ranging from small fractions of a second to many years.

<span class="mw-page-title-main">Neutron cross section</span> Measure of neutron interaction likelihood

In nuclear physics, the concept of a neutron cross section is used to express the likelihood of interaction between an incident neutron and a target nucleus. The neutron cross section σ can be defined as the area in cm2 for which the number of neutron-nuclei reactions taking place is equal to the product of the number of incident neutrons that would pass through the area and the number of target nuclei. In conjunction with the neutron flux, it enables the calculation of the reaction rate, for example to derive the thermal power of a nuclear power plant. The standard unit for measuring the cross section is the barn, which is equal to 10−28 m2 or 10−24 cm2. The larger the neutron cross section, the more likely a neutron will react with the nucleus.

Caesium (55Cs) has 41 known isotopes, the atomic masses of these isotopes range from 112 to 152. Only one isotope, 133Cs, is stable. The longest-lived radioisotopes are 135Cs with a half-life of 1.33 million years, 137
Cs
with a half-life of 30.1671 years and 134Cs with a half-life of 2.0652 years. All other isotopes have half-lives less than 2 weeks, most under an hour.

Naturally occurring zirconium (40Zr) is composed of four stable isotopes (of which one may in the future be found radioactive), and one very long-lived radioisotope (96Zr), a primordial nuclide that decays via double beta decay with an observed half-life of 2.0×1019 years; it can also undergo single beta decay, which is not yet observed, but the theoretically predicted value of t1/2 is 2.4×1020 years. The second most stable radioisotope is 93Zr, which has a half-life of 1.53 million years. Thirty other radioisotopes have been observed. All have half-lives less than a day except for 95Zr (64.02 days), 88Zr (83.4 days), and 89Zr (78.41 hours). The primary decay mode is electron capture for isotopes lighter than 92Zr, and the primary mode for heavier isotopes is beta decay.

Natural nitrogen (7N) consists of two stable isotopes: the vast majority (99.6%) of naturally occurring nitrogen is nitrogen-14, with the remainder being nitrogen-15. Thirteen radioisotopes are also known, with atomic masses ranging from 9 to 23, along with three nuclear isomers. All of these radioisotopes are short-lived, the longest-lived being nitrogen-13 with a half-life of 9.965(4) min. All of the others have half-lives below 7.15 seconds, with most of these being below 620 milliseconds. Most of the isotopes with atomic mass numbers below 14 decay to isotopes of carbon, while most of the isotopes with masses above 15 decay to isotopes of oxygen. The shortest-lived known isotope is nitrogen-10, with a half-life of 143(36) yoctoseconds, though the half-life of nitrogen-9 has not been measured exactly.

Plutonium (94Pu) is an artificial element, except for trace quantities resulting from neutron capture by uranium, and thus a standard atomic weight cannot be given. Like all artificial elements, it has no stable isotopes. It was synthesized long before being found in nature, the first isotope synthesized being plutonium-238 in 1940. Twenty plutonium radioisotopes have been characterized. The most stable are plutonium-244 with a half-life of 80.8 million years; plutonium-242 with a half-life of 373,300 years; and plutonium-239 with a half-life of 24,110 years; and plutonium-240 with a half-life of 6,560 years. This element also has eight meta states; all have half-lives of less than one second.

<span class="mw-page-title-main">Fission products (by element)</span> Breakdown of nuclear fission results

This page discusses each of the main elements in the mixture of fission products produced by nuclear fission of the common nuclear fuels uranium and plutonium. The isotopes are listed by element, in order by atomic number.

<span class="mw-page-title-main">Photodisintegration</span> Disintegration of atomic nuclei from high-energy EM radiation

Photodisintegration is a nuclear process in which an atomic nucleus absorbs a high-energy gamma ray, enters an excited state, and immediately decays by emitting a subatomic particle. The incoming gamma ray effectively knocks one or more neutrons, protons, or an alpha particle out of the nucleus. The reactions are called (γ,n), (γ,p), and (γ,α).

<span class="mw-page-title-main">Nuclear drip line</span> Atomic nuclei decay delimiter

The nuclear drip line is the boundary beyond which atomic nuclei are unbound with respect to the emission of a proton or neutron.

<span class="mw-page-title-main">Nuclear transmutation</span> Conversion of an atom from one element to another

Nuclear transmutation is the conversion of one chemical element or an isotope into another chemical element. Nuclear transmutation occurs in any process where the number of protons or neutrons in the nucleus of an atom is changed.

References

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  2. Morrison, P. (1958). "On gamma-ray astronomy". Il Nuovo Cimento. 7 (6): 858–865. Bibcode:1958NCim....7..858M. doi:10.1007/BF02745590. S2CID   121118803.
  3. Chupp, E.; et al. (1973). "Solar Gamma Ray and Neutron Observations". NASA Special Publication. 342: 285. Bibcode:1973NASSP.342..285C.
  4. Prompt Gamma-ray Neutron Activation Analysis. International Atomic Energy Agency
  5. D. Franklin; R. B. Adamson (1 January 1984). Zirconium in the Nuclear Industry: Sixth International Symposium. ASTM International. pp. 26–. ISBN   978-0-8031-0270-5 . Retrieved 7 October 2012.