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Fission product yield


Mass vs. yield curve

File:Fission yield volatile.png
From Fluoride volatility: Blue elements have volatile fluorides or are already volatile; green elements do not but have volatile chlorides; red elements have neither, but the elements themselves are volatile at very high temperatures. Yields at 100,1,2,3 years after fission, not considering later neutron capture, fraction of 100% not 200%. Beta decay Kr-85Rb, Sr-90Zr, Ru-106Pd, Sb-125Te, Cs-137Ba, Ce-144Nd, Sm-151Eu, Eu-155Gd visible.
File:ThermalFissionYield.svg
Fission product yields by mass for thermal neutron fission of U-235, Pu-239, a combination of the two typical of current nuclear power reactors, and U-233 used in the thorium cycle

If a graph of the mass or mole yield of fission products against the atomic number of the fragments is drawn then it has two peaks, one in the area zirconium through to palladium and one at xenon through to neodymium. This is because the fission event causes the nucleus to split in an asymmetric manner.[1]

Yield vs. Z – This is a typical distribution for the fission of uranium. Note that in the calculations used to make this graph the activation of fission products was ignored and the fission was assumed to occur in a single moment rather than a length of time. In this bar chart results are shown for different cooling times (time after fission).

Because of the stability of nuclei with even numbers of protons and/or neutrons the curve of yield against element is not a smooth curve. It tends to alternate.

In general, the higher the energy of the state that undergoes nuclear fission, the more likely a symmetric fission is, hence as the neutron energy increases and/or the energy of the fissile atom increases, the valley between the two peaks becomes more shallow; for instance, the curve of yield against mass for Pu-239 has a more shallow valley than that observed for U-235, when the neutrons are thermal neutrons. The curves for the fission of the later actinides tend to make even more shallow valleys. In extreme cases such as 259Fm, only one peak is seen.


Yield is usually expressed relative to number of fissioning nuclei, not the number of fission product nuclei, that is, yields should sum to 200%.

The table in the next section gives yields for notable radioactive (with halflife greater than one year, plus iodine-131) fission products, and (the few most absorptive) neutron poison fission products, from thermal neutron fission of U-235 (typical of nuclear power reactors), computed from [2].

The yields in the table sum to only 45.5522%, including 34.8401% which have halflife greater than one year:

t½ in years yield
1 to 5 2.7252%
10 to 100 12.5340%
2 to 300,000 6.1251%
1.5 to 16 million 13.4494%

The remainder and the unlisted 154.4478% decay with halflife less than one year into nonradioactive nuclei.

This is before accounting for the effects of any subsequent neutron capture, e.g.:

  • 135Xe capturing a neutron and becoming nonradioactive 136Xe, rather than decaying to 135Cs which is radioactive with a halflife of 2.3 million years
  • Nonradioactive 133Cs capturing a neutron and becoming 134Cs which is radioactive with a halflife of 2 years
  • Many of the fission products with mass 147 or greater such as Promethium-147, Samarium-149, Samarium-151, Europium-155 have significant cross sections for neutron capture, so that one heavy fission product atom can undergo multiple successive neutron captures.

Besides fission products, the other types of radioactive products are

Ordered by yield (thermal neutron fission of U-235)

Ordered by yield (thermal neutron fission of U-235)

Yield Isotope Halflife Comment
6.7896% 133Cs 134Cs 2.065y neutron capture (29 barns) slowly converts stable 133Cs to 134Cs, which itself is low-yield because beta decay stops at 134Xe; can be further converted (140 barns) to 135Cs
6.3333% 135I 135Xe 6.57h most important neutron poison; neutron capture converts 10%-50% of 135Xe to 136Xe; remainder decays (9.14h) to 135Cs (2.3my)
6.2956% 93Zr 1.53my
6.0899% 137Cs 30.17y
6.0507% 99Tc 211ky Candidate for disposal by nuclear transmutation
5.7518% 90Sr 28.9y
2.8336% 131I 8.02d
2.2713% 147Pm 2.62y
1.0888% 149Sm nonradioactive 2nd most significant neutron poison
0.6576% 129I 15.7my Candidate for disposal by nuclear transmutation
0.4203% 151Sm 90y neutron poison; most will be converted to stable 152Sm
0.3912% 106Ru 373.6d
0.2717% 85Kr 10.78y
0.1629% 107Pd 6.5my
0.0508% 79Se 295ky
0.0330% 155Eu 155Gd 4.76y both neutron poisons, most will be destroyed while fuel still in use
0.0297% 125Sb 2.76y
0.0236% 126Sn 230ky
0.0065% 157Gd nonradioactive neutron poison
0.0003% 113mCd 14.1y neutron poison, most will be destroyed while fuel still in use
File:Fission yield.png
Yields at 100,1,2,3 years after fission, probably of Pu-239 not U-235 because left hump is shifted right, not considering later neutron capture, fraction of 100% not 200%. Beta decay Kr-85Rb, Sr-90Zr, Ru-106Pd, Sb-125Te, Cs-137Ba, Ce-144Nd, Sm-151Eu, Eu-155Gd visible.

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Uranium-235 is an isotope of uranium that differs from the element’s other common isotope, uranium-238, by its ability to cause a rapidly expanding fission chain reaction, i.e., it is fissile. It is the only fissile isotope found in any economic quantity in nature. It was discovered in 1935 by Arthur Jeffrey Dempster.

If at least one neutron from U-235 fission strikes another nucleus and causes it to fission, then the chain reaction will continue. If the reaction will sustain itself, it is said to be critical, and the mass of U-235 required to produce the critical condition is said to be a critical mass. A critical chain reaction can be achieved at low concentrations of U-235 if the neutrons from fission are moderated to lower their speed, since the probability for fission with slow neutrons is greater. A fission chain reaction produces intermediate mass fragments which are highly radioactive and produce further energy by their radioactive decay. Some of them produce neutrons, called delayed neutrons, which contribute to the fission chain reaction. In nuclear reactors, the reaction is slowed down by the addition of control rods which are made of elements such as boron, cadmium, and hafnium which can absorb a large number of neutrons. In nuclear bombs, the reaction is uncontrolled and the large amount of energy released creates a nuclear explosion.

File:1940-Laurence-uranium235.png
The May 5, 1940 front-page New York Times article citing the power of uranium-235.

The fission of one atom of U-235 generates 200 MeV = 3.2 × 10<sup­>-11 J, i.e. 18 TJ/mol = 77 TJ/kg. However, approximately 5% of this energy is carried away by virtually undetectable neutrinos. [1]

The nuclear cross section for slow thermal neutrons is about 1000 barns. For fast neutrons it is in the order of 1 barn. [1]

Only around 0.72% of all natural uranium is uranium-235, the rest being mostly uranium-238. This concentration is insufficient for a self sustaining reaction in a light water reactor; enrichment, which just means separating out the uranium-238, must take place to get a usable concentration of uranium-235. Pressurised Heavy Water Reactors, other heavy water reactors, and some graphite moderated reactors are known for using unenriched uranium. Uranium which has been processed to boost its uranium-235 proportion is known as enriched uranium, different applications require unique levels of enrichment.

The fissile uranium in nuclear weapons usually contains 85% or more of 235U known as weapon(s)-grade, though for a crude, inefficient weapon 20% is sufficient (called weapon(s)-usable); even less is sufficient, but then the critical mass required rapidly increases. However, judicious use of implosion and neutron reflectors can enable construction of a weapon from a quantity of uranium below the usual critical mass for its level of enrichment, though this would likely only be possible in a country which already had extensive experience in developing nuclear weapons. The Little Boy atomic bomb was fueled by enriched uranium. Most modern nuclear arsenals use plutonium as the fissile component, however U-235 devices remain a nuclear proliferation concern due to the simplicity of this nuclear weapon design.

Uranium-235 has a half-life of 700 million years.

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See also

References

bg:Уран-235 da:Uran-235 id:Uranium-235 he:אורניום-235 no:Uran-235 Template:WH Template:WS

Ordered by mass number

Ordered by mass number

Yield Isotope
0.0508% style=”background:Template:Element color/Nonmetals” | selenium-79
0.2717% style=”background:Template:Element color/Noble gases” | krypton-85
5.7518% style=”background:Template:Element color/Alkaline earth metals” | strontium-90
6.2956% style=”background:Template:Element color/Transition metals” | zirconium-93
6.0507% style=”background:Template:Element color/Transition metals” | technetium-99
0.3912% style=”background:Template:Element color/Transition metals” | ruthenium-106
0.1629% style=”background:Template:Element color/Transition metals” | palladium-107
0.0003% style=”background:Template:Element color/Transition metals” | cadmium-113m
0.0297% style=”background:Template:Element color/Metalloids” | antimony-125
0.0236% style=”background:Template:Element color/Poor metals” | tin-126
0.6576% style=”background:Template:Element color/Halogens” | iodine-129
2.8336% style=”background:Template:Element color/Halogens” | iodine-131
6.7896% style=”background:Template:Element color/Alkali metals” | caesium-133 style=”background:Template:Element color/Alkali metals” | caesium-134
6.3333% style=”background:Template:Element color/Halogens” | iodine-135 style=”background:Template:Element color/Noble gases” | xenon-135 style=”background:Template:Element color/Alkali metals” | caesium-135
6.0899% style=”background:Template:Element color/Alkali metals” | caesium-137
2.2713% style=”background:Template:Element color/Lanthanides” | promethium-147
1.0888% style=”background:Template:Element color/Lanthanides” | samarium-149
0.4203% style=”background:Template:Element color/Lanthanides” | samarium-151
0.0330% style=”background:Template:Element color/Lanthanides” | europium-155 style=”background:Template:Element color/Lanthanides” | gadolinium-155
0.0065% style=”background:Template:Element color/Lanthanides” | gadolinium-157
Ordered by halflife

Ordered by halflife

Yield Isotope Halflife Comment
2.8336% 131I 8.02d Important in nuclear explosions and accidents but not in cooled spent nuclear fuel
0.3912% 106Ru 373.6d
6.7896% 133Cs 134Cs 2.065y neutron capture converts a few percent of nonradioactive 133Cs to 134Cs, which has low direct yield because beta decay stops at 134Xe
2.2713% 147Pm 2.62y
0.0297% 125Sb 2.76y
<0.0330% 155Eu 155Gd 4.76y both neutron poisons, most will be destroyed by neutron capture while still in reactor
0.2717% 85Kr 10.78y Current nuclear reprocessing releases it to atmosphere
<0.0003% 113mCd 14.1y most will be destroyed by neutron capture while still in reactor
5.7518% 90Sr 28.9y One of two principal medium-term radiation and heat sources
6.0899% 137Cs 30.17y One of two principal medium-term radiation and heat sources
<0.4203% 151Sm 90y Most will be destroyed by neutron capture while still in reactor
6.0507% 99Tc 211ky Dominant radiation source among FP in period about Template:E to Template:E years; mobile in environment; candidate for disposal by nuclear transmutation
0.0236% 126Sn 230ky
0.0508% 79Se 295ky
6.2956% 93Zr 1.53my
<6.3333% 135Cs 2.3my
0.1629% 107Pd 6.5my
0.6576% 129I 15.7my Mobile in environment; candidate for disposal by nuclear transmutation
<1.0888% 149Sm nonradioactive neutron poison
<0.0065% 157Gd nonradioactive neutron poison

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]


Overview

The half-life of a quantity, subject to exponential decay, is the time required for the quantity to decay to half of its initial value. The concept originated in the study of radioactive decay, but applies to many other fields as well, including phenomena which are described by non-exponential decays.

The term half-life was coined in 1907, but it was always referred to as half-life period. It was not until the early 1950s that the word period was dropped from the name. [1]

Number of
half-lives
elapsed
Fraction
remaining
As
power
of 2
0 1/1 <math>1/2^0</math>
1 1/2 <math>1/2^1</math>
2 1/4 <math>1/2^2</math>
3 1/8 <math>1/2^3</math>
4 1/16 <math>1/2^4</math>
5 1/32 <math>1/2^5</math>
6 1/64 <math>1/2^6</math>
7 1/128 <math>1/2^7</math>
<math>N</math> <math>1/2^N</math> <math>1/2^N</math>

The table at right shows the reduction of the quantity in terms of the number of half-lives elapsed.

It can be shown that, for exponential decay, the half-life <math>t_{1/2}</math> obeys this relation:

<math>

t_{1/2} = \frac{\ln (2)}{\lambda} </math> where

  • <math>\ln (2)</math> is the natural logarithm of 2 (approximately 0.693), and
  • λ is the decay constant, a positive constant used to describe the rate of exponential decay.

The half-life is related to the mean lifetime τ by the following relation:

<math> t_{1/2} = \ln (2) \cdot \tau </math>

Examples

The constant <math>\lambda</math> can represent many different specific physical quantities, depending on what process is being described.

  • In an RC circuit or RL circuit, <math>\lambda</math> is the reciprocal of the circuit’s time constant. For simple RC and RL circuits, <math>\lambda</math> equals <math>1/RC</math> or <math>R/L</math>, respectively.
  • In first-order chemical reactions, <math>\lambda</math> is the reaction rate constant.
  • In radioactive decay, it describes the probability of decay per unit time: <math>dN = \lambda N dt</math>, where dN is the number of nuclei decayed during the time dt, and N is the quantity of radioactive nuclei.
  • In biology (specifically pharmacokinetics), from MeSH: Half-Life: The time it takes for a substance (drug, radioactive nuclide, or other) to lose half of its pharmacologic, physiologic, or radiologic activity. Year introduced: 1974 (1971).

Decay by two or more processes

Some quantities decay by two processes simultaneously (see Decay by two or more processes). In a fashion similar to the previous section, we can calculate the new total half-life <math>T_{1/2}</math> and we’ll find it to be:

<math>T_{1/2} = \frac{\ln 2}{\lambda _1 + \lambda _2} \,</math>

or, in terms of the two half-lives <math>t_1</math> and <math>t_2</math>

<math>T_{1/2} = \frac{t _1 t _2}{t _1 + t_2} \,</math>

i.e., half their harmonic mean.

Derivation

Quantities that are subject to exponential decay are commonly denoted by the symbol <math>N</math>. (This convention suggests a decaying number of discrete items. This interpretation is valid in many, but not all, cases of exponential decay.) If the quantity is denoted by the symbol <math>N</math>, the value of <math>N</math> at a time <math>t</math> is given by the formula:

<math>N(t) = N_0 e^{-\lambda t} \,</math>

where <math>N_0</math> is the initial value of <math>N</math> (at <math>t = 0</math>)

When <math>t = 0</math>, the exponential is equal to 1, and <math>N(t)</math> is equal to <math>N_0</math>. As <math>t</math> approaches infinity, the exponential approaches zero. In particular, there is a time <math>t_{1/2} \,</math> such that

<math>N(t_{1/2}) = N_0\cdot\frac{1}{2}. </math>

Substituting into the formula above, we have

<math>N_0\cdot\frac{1}{2} = N_0 e^{-\lambda t_{1/2}}, \,</math>
<math>e^{-\lambda t_{1/2}} = \frac{1}{2}, \,</math>
<math>- \lambda t_{1/2} = \ln \frac{1}{2} = – \ln{2}, \,</math>
<math>t_{1/2} = \frac{\ln 2}{\lambda}. \,</math>

Experimental determination

The half-life of a process can be determined easily by experiment. In fact, some methods do not require advance knowledge of the law governing the decay rate, be it exponential decay or another pattern.

Most appropriate to validate the concept of half-life for radioactive decay, in particular when dealing with a small number of atoms, is to perform experiments and correct computer simulations. See in [2] how to test the behavior of the last atoms. Validation of physics-math models consists in comparing the model’s behavior with experimental observations of real physical systems or valid simulations (physical and/or computer). The references given here describe how to test the validity of the exponential formula for small number of atoms with simple simulations, experiments, and computer code.

In radioactive decay, the exponential model does not apply for a small number of atoms (or a small number of atoms is not within the domain of validity of the formula or equation or table). The DIY experiments use pennies or M&M’s candies. [3], [4]. A similar experiment is performed with isotopes of a very short half-life, for example, see Fig 5 in [5]. See how to write a computer program that simulates radioactive decay including the required randomness in [6] and experience the behavior of the last atoms. Of particular note, atoms undergo radioactive decay in whole units, and so after enough half-lives the remaining original quantity becomes an actual zero rather than asymptotically approaching zero as with continuous systems.

See also

References

  1. John Ayto “20th Century Words” (1999) Cambridge University Press.


af:Halfleeftyd ar:عمر النصف ast:Periodu de semidesintegración ca:Període de semidesintegració cs:Poločas přeměny da:Halveringstid de:Halbwertszeit et:Poolestusaeg eo:Duoniĝtempo eu:Semidesintegrazio-periodo fa:نیمه عمر ko:반감기 id:Waktu paruh is:Helmingunartími it:Emivita (fisica) he:מחצית חיים lt:Pusėjimo trukmė hu:Felezési idő nl:Halfwaardetijd no:Halveringstid nn:Halveringstid sr:Време полураспада fi:Puoliintumisaika sv:Halveringstid ta:அரைவாழ்வுக் காலம் th:ครึ่งชีวิต

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Ordered by thermal neutron neutron absorption cross section
Barns Yield Isotope t½ Comment
2650000 6.3333% 135I 135Xe 6.57h Most important neutron poison; neutron capture rapidly converts 135Xe to 136Xe; remainder decays (9.14h) to 135Cs (2.3my)
254000 0.0065% 157Gd neutron poison, but low yield
40140 1.0888% 149Sm 2nd most important neutron poison
20600 0.0003% 113mCd 14.1y most will be destroyed by neutron capture
15200 0.4203% 151Sm 90y most will be destroyed by neutron capture
3950 0.0330% 155Eu 155Gd 4.76y both neutron poisons
96 2.2713% 147Pm 2.62y
80 2.8336% 131I 8.02d
29
140
6.7896% 133Cs 134Cs
2.065y
neutron capture converts a few percent of nonradioactive 133Cs to 134Cs, which has very low direct yield because beta decay stops at 134Xe; further capture will add to long-lived 135Cs
20 6.0507% 99Tc 211ky candidate for disposal by nuclear transmutation
18 0.6576% 129I 15.7my candidate for disposal by nuclear transmutation
2.7 6.2956% 93Zr 1.53my transmutation impractical
1.8 0.1629% 107Pd 6.5my
1.66 0.2717% 85Kr 10.78y
0.90 5.7518% 90Sr 28.9y
0.15 0.3912% 106Ru 373.6d
0.11 6.0899% 137Cs 30.17y
0.0297% 125Sb 2.76y
0.0236% 126Sn 230ky
0.0508% 79Se 295ky
References

References

  • Chain Fission Yields For 90-Th-232 92-U-233 92-U-235 92-U-238 94-Pu-239 94-Pu-241, and Thermal, Fast, 14MeV.

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