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Fission products (by element)
Krypton-85 is formed by the fission process with a fission yield of about 0.3%. Only 20% of the fission products of mass 85 become 85Kr itself; the rest passes through a short-lived nuclear isomer and then to stable 85Rb. During the fuel dissolution this radioactive krypton is released into the air. This krypton release can be detected and used as a means of detecting clandestine nuclear reprocessing. Strictly speaking, the stage which is detected is the dissolution of used nuclear fuel in nitric acid, as it is at this stage that the krypton and other fission gases like the more abundant xenon are released.
Increase of fission gases above a certain limit can lead to fuel pin swelling and even puncture, so that fission gas measurement after discharging the fuel from reactor is most important to make burn-up calculations, to study the nature of fuel inside the reactor, behaviour with pin materials, for effective utilisation of fuel and also reactor safety.
While the atom yield of strontium is low, the strontium radioisotopes are very important as strontium is a calcium mimic which is incorporated in bone growth and therefore has a great ability to harm humans. On the other hand, this also allows 89Sr to be used in the open source radiotherapy of bone tumors. This tends to be used in palliative care to reduce the pain due to secondary tumors in the bones.
The only stable yttrium isotope, 89Y, will be found with yield somewhat less than 1% in a fission product mixture which has been allowed to age for months or years, as the other isotopes have half-lives of 106.6 days or less.
90Sr decays into 90Y which is a beta emitter with a half life of 2.67 days. 90Y is sometimes used for medical purposes and can be obtained either by the neutron activation of stable 89Y or by using a device similar to a technetium cow.
A significant amount of zirconium is formed by the fission process; some of this are shortlived radioactives (95Zr and 97Zr which decay to molybdenum), while almost 10% of the fission products mixture after years of decay is five stable or extremely longlived isotopes of zirconium, and 93Zr with a halflife of 1.53 million years.
In PUREX plants the zirconium sometimes forms a third phase which can be a disturbance in the plant. The third phase is the term in solvent extraction given to a third layer (such as foam and/or emulsion) which forms from the two layers in the solvent extraction process. The zirconium forms the third phase by forming small particles which stabilise the emulsion which is the third phase.
Molybdenum 95, 97, 98, 100
The fission product mixture contains significant amounts of molybdenum.
Plenty of both stable ruthenium and radioactive ruthenium-103 is formed by the fission process. The ruthenium in PUREX raffinate can become oxidized to form ruthenium tetroxide which forms a purple vapour to appear above the surface of the aqueous liquor. The ruthenium tetroxide is very similar to osmium tetroxide, the ruthenium compound is a stronger oxidant which enables it to form deposits by reacting with other substances. In this way the ruthenium in a reprocessing plant is very mobile and can be found in odd places. Also at Chernobyl during the fire the ruthenium became volatile and behaved differently to many of the other metallic fission products. Some of the particles which were emitted by the fire were very rich in ruthenium.
In addition the ruthenium in PUREX raffinate forms a large number of nitrosyl complexes which makes the chemistry of the ruthenium very complex. The ligand exchange rate at ruthenium and rhodium tends to be long, hence it can take a long time for a ruthenium or rhodium compound to react.
It has been suggested that the ruthenium and palladium in PUREX raffinate should be used as a source of the metals .
While less rhodium than ruthenium and palladium is formed (around 3.6% yield), the mixture of fission products still contains a significant amount of this metal. Due to the high prices of ruthenium, rhodium and palladium some work has been done on the separation of these metals to enable them to be used at a later date. Because of the possibility of the metals being contaminated by radioactive isotopes, metals are not suitable for making consumer products such as jewellery but this source of the metals could be used for catalysts in industrial plants such as petrochemical plants.
Potential Applications of Fission Platinoids in Industry, Zdenek Kolarik, Platinum Metals Review, 2005, 49, April (2).
A dire example of people being exposed to radiation from contaminated jewellery occurred in the USA where it is thought that the gold seeds which were used to contain radon were recycled into jewellery. The gold did contain radioactive decay products of 222Rn. Further details can be found at  and .
A great deal of palladium forms during the fission process, during the fuel dissolution not all of the fission palladium dissolves. Hence the dissolver fines are rich in palladium, also some palladium dissolves at first and then comes out of solution again. The dissolver fines are often removed to prevent them disturbing the solvent extraction process through the stabilisation of the third phase.
The fission palladium can separate during the process in which the PUREX raffinate is combined with glass and heated to form the final waste form. The palladium forms an alloy with the fission tellurium. This alloy can separate from the glass.
Tellurium 125, 128, 130
Tellurium-132 and its daughter 132I are important in the first few days after a criticality. It was responsible for a large fraction of the dose inflicted on workers at Chernobyl in the first week.
The isobar forming 132Te/132I is
Iodine 129, 131
Several iodine radioisotopes are made by the fission process, please see below for more details. In common with 89Sr, 131I is used for the treatment of cancer. A small dose of 131I can be used in a thyroid function test while a large dose can be used to destroy the thyroid tissue. This treatment will also normally seek out and destroy any secondary tumor which arose from a thyroid cancer. Much of the energy from the beta emission from the 131I will be absorbed in the thyroid, while the gamma rays are likely to be able to escape from the thyroid to irradiate other parts of the body.
Lots of 131I was released during an experiment named the 'Green run'. The 'green run' was an experiment in which fuel which had only been allowed to cool for a short time after irradiation was reprocessed in a plant which had no iodine scrubber in operation.
In reactor fuel the fission xenon tends to migrate to form bubbles in the fuel. As cesium 133, 135, and 137 are formed by the beta particle decay of the corresponding xenon isotopes, this causes the cesium to become physically separated from the bulk of the uranium oxide fuel.
Because 135Xe is a potent nuclear poison with a large cross section for neutron absorption, the buildup of xenon in the fuel inside a power reactor can lower the reactivity greatly. If a power reactor is shut down or left running at a low power, then large amounts of xenon 135 can build up through decay of 135I. When the 135Xe has been consumed through neutron capture reactions, the reactivity of the core will increase. In some fuels, boron is added as a burnable poison to decrease the reactivity of the nuclear fuel; these boron loaded fuels are intended to give the same reactivity throughout the time it is in the reactor core.
It is thought that xenon poisoning was one of the factors which lead to the power surge which damaged the Chernobyl reactor core.
Cesium 133, 134, 135, 137
A lot of cesium is formed by the fission process, please see the section in the main fission product page for further details of cesium as a troublesome isotope in fall-out and nuclear wastes. This element is a key element which allows the fission products from a bomb to be distinguished from power reactor fission products.
A map of cesium-137 in the area around Chernobyl has been published by the IAEA.
Barium 138, 139
A lot of barium is formed by the fission process, a short lived barium isotope was confused with radium by some early workers. They were bombarding uranium with neutrons in an attempt to form a new element. But instead they caused fission which generated a large amount of radioactivity in the target. Because the chemistry of barium and radium the two elements could be coseparated by for instance a precipitation with sulphate anions. Because of this similarity of their chemistry the early workers thought that the very radioactive fraction which was separated into the "radium" fraction contained a new isotope of radium. Some of this early work was done by Otto Hahn and Strassmann.
Lanthanides (lanthanum 139, cerium 140-144, neodymium 142-146, 148, 150, promethium-147, and samarium 149, 151, 152, 154)
A great deal of the lighter lanthanides (lanthanum, cerium, neodymium, and samarium) are formed as fission products. It is interesting to note that in Africa at Oklo where the natural nuclear fission reactor operated millions of years ago the isotopic mixture of neodymium is not the same as 'normal' neodymium, it has an isotope pattern very similar to the neodymium formed by fission.
In the aftermath of criticality accidents the level of 140La is often used to determine the fission yield (in terms of the number of nuclei which underwent fission).
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Fission_products_(by_element)". A list of authors is available in Wikipedia.|