Pleochroic halo

Last updated
Pleochroic halos around crystals of zircons in a sample of biotite Dark crown.JPG
Pleochroic halos around crystals of zircons in a sample of biotite

A pleochroic halo, or radiohalo, is a microscopic, spherical shell of discolouration (pleochroism) within minerals such as biotite that occurs in granite and other igneous rocks. The halo is a zone of radiation damage caused by the inclusion of minute radioactive crystals within the host crystal structure. The inclusions are typically zircon, apatite, or titanite which can accommodate uranium or thorium within their crystal structures. [1] One explanation is that the discolouration is caused by alpha particles emitted by the nuclei; the radius of the concentric shells are proportional to the particles' energy. [2]

Contents

Production

Uranium-238 follows a sequence of decay through thorium, radium, radon, polonium, and lead. These are the alpha-emitting isotopes in the sequence. (Because of their continuous energy distribution and greater range, beta particles cannot form distinct rings.)

Isotope Half-life Energy in MeV
U-2384.47×109 years4.196
U-2342.455×105 years4.776
Th-23075,400 years4.6876
Ra-2261,599 years4.784
Rn-2223.823 days5.4897
Po-2183.04 minutes5.181
Po-214163.7 microseconds7.686
Po-210138.4 days5.304
Pb-206stable0

The final characteristics of a pleochroic halo depends upon the initial isotope, and the size of each ring of a halo is dependent upon the alpha decay energy. A pleochroic halo formed from U-238 has theoretically eight concentric rings, with five actually distinguishable under a lighted microscope, while a halo formed from polonium has only one, two, or three rings depending on which isotope the starting material is. [3] In U-238 haloes, U-234, and Ra-226 rings coincide with the Th-230 to form one ring; Rn-222 and Po-210 rings also coincide to form one ring. These rings are indistinguishable from one another under a petrographic microscope. [4]

Related Research Articles

The actinide or actinoid series encompasses at least the 14 metallic chemical elements in the 5f series, with atomic numbers from 89 to 102, actinium through nobelium. The actinide series derives its name from the first element in the series, actinium. The informal chemical symbol An is used in general discussions of actinide chemistry to refer to any actinide.

<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">Protactinium</span> Chemical element with atomic number 91 (Pa)

Protactinium is a chemical element; it has symbol Pa and atomic number 91. It is a dense, radioactive, silvery-gray actinide metal which readily reacts with oxygen, water vapor, and inorganic acids. It forms various chemical compounds, in which protactinium is usually present in the oxidation state +5, but it can also assume +4 and even +3 or +2 states. Concentrations of protactinium in the Earth's crust are typically a few parts per trillion, but may reach up to a few parts per million in some uraninite ore deposits. Because of its scarcity, high radioactivity, and high toxicity, there are currently no uses for protactinium outside scientific research, and for this purpose, protactinium is mostly extracted from spent nuclear fuel.

<span class="mw-page-title-main">Polonium</span> Chemical element with atomic number 84 (Po)

Polonium is a chemical element; it has symbol Po and atomic number 84. A rare and highly radioactive metal with no stable isotopes, polonium is a chalcogen and chemically similar to selenium and tellurium, though its metallic character resembles that of its horizontal neighbors in the periodic table: thallium, lead, and bismuth. Due to the short half-life of all its isotopes, its natural occurrence is limited to tiny traces of the fleeting polonium-210 in uranium ores, as it is the penultimate daughter of natural uranium-238. Though longer-lived isotopes exist, such as the 124 years half-life of polonium-209, they are much more difficult to produce. Today, polonium is usually produced in milligram quantities by the neutron irradiation of bismuth. Due to its intense radioactivity, which results in the radiolysis of chemical bonds and radioactive self-heating, its chemistry has mostly been investigated on the trace scale only.

A radionuclide (radioactive nuclide, radioisotope or radioactive isotope) is a nuclide that has excess numbers of either neutrons or protons, giving it excess nuclear energy, and making it unstable. This excess energy can be used in one of three ways: emitted from the nucleus as gamma radiation; transferred to one of its electrons to release it as a conversion electron; or used to create and emit a new particle (alpha particle or beta particle) from the nucleus. During those processes, the radionuclide is said to undergo radioactive decay. These emissions are considered ionizing radiation because they are energetic enough to liberate an electron from another atom. The radioactive decay can produce a stable nuclide or will sometimes produce a new unstable radionuclide which may undergo further decay. Radioactive decay is a random process at the level of single atoms: it is impossible to predict when one particular atom will decay. However, for a collection of atoms of a single nuclide the decay rate, and thus the half-life (t1/2) for that collection, can be calculated from their measured decay constants. The range of the half-lives of radioactive atoms has no known limits and spans a time range of over 55 orders of magnitude.

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">Decay chain</span> Series of radioactive decays

In nuclear science, the decay chain refers to a series of radioactive decays of different radioactive decay products as a sequential series of transformations. It is also known as a "radioactive cascade". The typical radioisotope does not decay directly to a stable state, but rather it decays to another radioisotope. Thus there is usually a series of decays until the atom has become a stable isotope, meaning that the nucleus of the atom has reached a stable state.

<span class="mw-page-title-main">Uranium-238</span> Isotope of uranium

Uranium-238 is the most common isotope of uranium found in nature, with a relative abundance of 99%. Unlike uranium-235, it is non-fissile, which means it cannot sustain a chain reaction in a thermal-neutron reactor. However, it is fissionable by fast neutrons, and is fertile, meaning it can be transmuted to fissile plutonium-239. 238U cannot support a chain reaction because inelastic scattering reduces neutron energy below the range where fast fission of one or more next-generation nuclei is probable. Doppler broadening of 238U's neutron absorption resonances, increasing absorption as fuel temperature increases, is also an essential negative feedback mechanism for reactor control.

Polonium-210 (210Po, Po-210, historically radium F) is an isotope of polonium. It undergoes alpha decay to stable 206Pb with a half-life of 138.376 days (about 4+12 months), the longest half-life of all naturally occurring polonium isotopes (210–218Po). First identified in 1898, and also marking the discovery of the element polonium, 210Po is generated in the decay chain of uranium-238 and radium-226. 210Po is a prominent contaminant in the environment, mostly affecting seafood and tobacco. Its extreme toxicity is attributed to intense radioactivity, mostly due to alpha particles, which easily cause radiation damage, including cancer in surrounding tissue. The specific activity of 210
Po
is 166 TBq/g, i.e., 1.66 × 1014 Bq/g. At the same time, 210Po is not readily detected by common radiation detectors, because its gamma rays have a very low energy. Therefore, 210
Po
can be considered as a quasi-pure alpha emitter.

Uranium–uranium dating is a radiometric dating technique which compares two isotopes of uranium (U) in a sample: uranium-234 (234U) and uranium-238 (238U). It is one of several radiometric dating techniques exploiting the uranium radioactive decay series, in which 238U undergoes 14 alpha and beta decay events on the way to the stable isotope 206Pb. Other dating techniques using this decay series include uranium–thorium dating and uranium–lead dating.

Uranium (92U) is a naturally occurring radioactive element (radioelement) with no stable isotopes. It has two primordial isotopes, uranium-238 and uranium-235, that have long half-lives and are found in appreciable quantity in Earth's crust. The decay product uranium-234 is also found. Other isotopes such as uranium-233 have been produced in breeder reactors. In addition to isotopes found in nature or nuclear reactors, many isotopes with far shorter half-lives have been produced, ranging from 214U to 242U. The standard atomic weight of natural uranium is 238.02891(3).

Protactinium (91Pa) has no stable isotopes. The four naturally occurring isotopes allow a standard atomic weight to be given.

Lead (82Pb) has four observationally stable isotopes: 204Pb, 206Pb, 207Pb, 208Pb. Lead-204 is entirely a primordial nuclide and is not a radiogenic nuclide. The three isotopes lead-206, lead-207, and lead-208 represent the ends of three decay chains: the uranium series, the actinium series, and the thorium series, respectively; a fourth decay chain, the neptunium series, terminates with the thallium isotope 205Tl. The three series terminating in lead represent the decay chain products of long-lived primordial 238U, 235U, and 232Th. Each isotope also occurs, to some extent, as primordial isotopes that were made in supernovae, rather than radiogenically as daughter products. The fixed ratio of lead-204 to the primordial amounts of the other lead isotopes may be used as the baseline to estimate the extra amounts of radiogenic lead present in rocks as a result of decay from uranium and thorium.

The environmental isotopes are a subset of isotopes, both stable and radioactive, which are the object of isotope geochemistry. They are primarily used as tracers to see how things move around within the ocean-atmosphere system, within terrestrial biomes, within the Earth's surface, and between these broad domains.

<span class="mw-page-title-main">Actinides in the environment</span>

The actinide series is a group of chemical elements with atomic numbers ranging from 89 to 102, including notable elements such as uranium and plutonium. The nuclides thorium-232, uranium-235, and uranium-238 occur primordially, while trace quantities of actinium, protactinium, neptunium, and plutonium exist as a result of radioactive decay and neutron capture of uranium. These elements are far more radioactive than the naturally occurring thorium and uranium, and thus have much shorter half-lives. Elements with atomic numbers greater than 94 do not exist naturally on Earth, and must be produced in a nuclear reactor. However, certain isotopes of elements up to californium still have practical applications which take advantage of their radioactive properties.

Uranium-236 (236U) is an isotope of uranium that is neither fissile with thermal neutrons, nor very good fertile material, but is generally considered a nuisance and long-lived radioactive waste. It is found in spent nuclear fuel and in the reprocessed uranium made from spent nuclear fuel.

Norman Feather FRS FRSE PRSE, was an English nuclear physicist. Feather and Egon Bretscher were working at the Cavendish Laboratory, Cambridge in 1940, when they proposed that the 239 isotope of element 94 (plutonium) would be better able to sustain a nuclear chain reaction. This research, a breakthrough, was part of the Tube Alloys project, the secret British project during World War II to develop nuclear weapons.

<span class="mw-page-title-main">Alpha particle</span> Ionizing radiation particle of two protons and two neutrons

Alpha particles, also called alpha rays or alpha radiation, consist of two protons and two neutrons bound together into a particle identical to a helium-4 nucleus. They are generally produced in the process of alpha decay but may also be produced in other ways. Alpha particles are named after the first letter in the Greek alphabet, α. The symbol for the alpha particle is α or α2+. Because they are identical to helium nuclei, they are also sometimes written as He2+ or 4
2
He
2+ indicating a helium ion with a +2 charge (missing its two electrons). Once the ion gains electrons from its environment, the alpha particle becomes a normal (electrically neutral) helium atom 4
2
He
.

<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.

<span class="mw-page-title-main">Discovery of nuclear fission</span> 1938 achievement in physics

Nuclear fission was discovered in December 1938 by chemists Otto Hahn and Fritz Strassmann and physicists Lise Meitner and Otto Robert Frisch. Fission is a nuclear reaction or radioactive decay process in which the nucleus of an atom splits into two or more smaller, lighter nuclei and often other particles. The fission process often produces gamma rays and releases a very large amount of energy, even by the energetic standards of radioactive decay. Scientists already knew about alpha decay and beta decay, but fission assumed great importance because the discovery that a nuclear chain reaction was possible led to the development of nuclear power and nuclear weapons. Hahn was awarded the 1944 Nobel Prize in Chemistry for the discovery of nuclear fission.

References

  1. Faure, Gunter (1986). Principles of Isotope Geology. Wiley. pp. 354–355.
  2. Henderson, G.H.; Bateson, S. (1934). "A Quantitative Study of Pleochroic Haloes, I". Proceedings of the Royal Society of London A. 145 (855): 563–581. Bibcode:1934RSPSA.145..563H. doi: 10.1098/rspa.1934.0120 . JSTOR   2935523.
  3. Weber, B. (2010). "Halos und weitere radioaktive Erscheinungen im Wölsendorfer Fluorit (in German)". Der Aufschluss. 61: 107–118.[ permanent dead link ]
  4. Pal, Dipak C. (2004). "Concentric rings of radioactive halo in chlorite, Turamdih uranium deposit, Singhbhum Shear Zone, Eastern India: a possible result of 238U chain decay". Current Science. 87 (5): 662–667.

Further reading

  1. Collins, L.G. (1997). "Polonium Halos and Myrmekite in Pegmatite and Granite". In Hunt, C. W.; Collins, L. G.; Skobelin, E. A. (eds.). Expanding Geospheres, Energy And Mass Transfers From Earth's Interior. Calgary: Polar Publishing Company. pp. 128–140.
  2. Durrani, S.A.; Fremlin, J.H.; Durrani, S. A. (1979). "Polonium Haloes in Mica". Nature. 278 (5702) (published October 1979): 333–335. Bibcode:1979Natur.278..333H. doi:10.1038/278333a0. S2CID   4260888.
  3. Henderson, G.H.; Bateson, S. (1934). "A Quantitative Study of Pleochroic Haloes, I". Proceedings of the Royal Society of London A. 145 (855): 563–581. Bibcode:1934RSPSA.145..563H. doi: 10.1098/rspa.1934.0120 . JSTOR   2935523.
  4. Henderson, G. H. (1939). "A quantitative study of pleochroic haloes. V. The genesis of haloes". Proceedings of the Royal Society of London A. 173 (953): 250–264. Bibcode:1939RSPSA.173..250H. doi: 10.1098/rspa.1939.0143 .
  5. Lide, D. R., ed. (2001). CRC Handbook of Chemistry and Physics (82nd ed.). Boca Raton, FL: CRC Press. ISBN   0-8493-0482-2.
  6. Moazed, C.; Spector, R. M.; Ward, R. F. (1973). "Polonium Radiohalos: An Alternate Interpretation". Science. 180 (4092): 1272–1274. Bibcode:1973Sci...180.1272M. doi:10.1126/science.180.4092.1272. PMID   17759119. S2CID   32535868.
  7. Odom, A. L.; Rink, W. J. (1989). "Giant Radiation-Induced Color Halos in Quartz: Solution to a Riddle". Science. 246 (4926): 107–109. Bibcode:1989Sci...246..107L. doi:10.1126/science.246.4926.107. PMID   17837769. S2CID   1639793.
  8. Schnier, C (2002). "Indications for the existence of superheavy elements in radioactive halos". Journal of Radioanalytical and Nuclear Chemistry. 253 (2): 209–216. doi:10.1023/A:1019633305770. S2CID   120109166.
  9. York, Derek (1979). "Polonium halos and geochronology". Eos, Transactions American Geophysical Union. 60 (33): 617–618. Bibcode:1979EOSTr..60..617Y. doi:10.1029/EO060i033p00617.