Metamictisation (sometimes called metamictization or metamiction) is a natural process resulting in the gradual and ultimately complete destruction of a mineral's crystal structure, leaving the mineral amorphous. The affected material is therefore described as metamict.
Certain minerals occasionally contain interstitial impurities of radioactive elements, and it is the alpha radiation emitted from those compounds that is responsible for degrading a mineral's crystal structure through internal bombardment. The effects of metamictisation are extensive: other than negating any birefringence previously present, the process also lowers a mineral's refractive index, hardness, and its specific gravity. The mineral's colour is also affected: metamict specimens are usually green, brown or blackish. Further, metamictisation diffuses the bands of a mineral's absorption spectrum. Curiously and inexplicably, the one attribute which metamictisation does not alter is dispersion. All metamict materials are themselves radioactive, some dangerously so.
An example of a metamict mineral is zircon. The presence of uranium and thorium atoms substituting for zirconium in the crystal structure is responsible for the radiation damage in this case. Unaffected specimens are termed high zircon while metamict specimens are termed low zircon. Other minerals known to undergo metamictisation include allanite, gadolinite, ekanite, thorite and titanite. Ekanite is almost invariably found completely metamict as thorium and uranium are part of its essential chemical composition.
Metamict minerals can have their crystallinity and properties restored through prolonged annealing.
A related phenomenon is the formation of pleochroic halos surrounding minute zircon inclusions within a crystal of biotite or other mineral. The spherical halos are produced by alpha particle radiation from the included uranium- or thorium-bearing species. Such halos can also be found surrounding monazite and other radioactive minerals.
Radiometric dating, radioactive dating or radioisotope dating is a technique which is used to date materials such as rocks or carbon, in which trace radioactive impurities were selectively incorporated when they were formed. The method compares the abundance of a naturally occurring radioactive isotope within the material to the abundance of its decay products, which form at a known constant rate of decay. The use of radiometric dating was first published in 1907 by Bertram Boltwood and is now the principal source of information about the absolute age of rocks and other geological features, including the age of fossilized life forms or the age of Earth itself, and can also be used to date a wide range of natural and man-made materials.
Thorium is a weakly radioactive metallic chemical element with the symbol Th and atomic number 90. Thorium is light silver and tarnishes olive gray when it is exposed to air, forming thorium dioxide; it is moderately soft and malleable and has a high melting point. Thorium is an electropositive actinide whose chemistry is dominated by the +4 oxidation state; it is quite reactive and can ignite in air when finely divided.
Zircon is a mineral belonging to the group of nesosilicates and is a source of the metal zirconium. Its chemical name is zirconium(IV) silicate, and its corresponding chemical formula is ZrSiO4. An empirical formula showing some of the range of substitution in zircon is (Zr1–y, REEy)(SiO4)1–x(OH)4x–y. Zircon precipitates from silicate melts and has relatively high concentrations of high field strength incompatible elements. For example, hafnium is almost always present in quantities ranging from 1 to 4%. The crystal structure of zircon is tetragonal crystal system. The natural color of zircon varies between colorless, yellow-golden, red, brown, blue, and green.
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. 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.
Pyrochlore2Nb2O6(OH,F) is a mineral group of the niobium end member of the pyrochlore supergroup. The general formula, A2B2O7, represent a family of phases isostructural to the mineral pyrochlore. Pyrochlores are an important class of materials in diverse technological applications such as luminescence, ionic conductivity, nuclear waste immobilization, high-temperature thermal barrier coatings, automobile exhaust gas control, catalysts, solid oxide fuel cell, ionic/electrical conductors etc.
Monazite is a primarily reddish-brown phosphate mineral that contains rare-earth elements. Due to variability in composition, monazite is considered a group of minerals. The most common species of the group is monazite-(Ce), that is, the cerium-dominant member of the group. It occurs usually in small isolated crystals. It has a hardness of 5.0 to 5.5 on the Mohs scale of mineral hardness and is relatively dense, about 4.6 to 5.7 g/cm3. There are five different most common species of monazite, depending on the relative amounts of the rare earth elements in the mineral:
Spontaneous fission (SF) is a form of radioactive decay that is found only in very heavy chemical elements. The nuclear binding energy of the elements reaches its maximum at an atomic mass number of about 56 ; spontaneous breakdown into smaller nuclei and a few isolated nuclear particles becomes possible at greater atomic mass numbers.
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.
Thorite, (Th,U)SiO4, is a rare nesosilicate of thorium that crystallizes in the tetragonal system and is isomorphous with zircon and hafnon. It is the most common mineral of thorium and is nearly always strongly radioactive. It was named in 1829 to reflect its thorium content. Thorite was discovered in 1828 on the island of Løvøya, Norway, by the vicar and mineralogist, Hans Morten Thrane Esmark, who sent the first specimens of this black mineral to his father, Jens Esmark, who was a professor of mineralogy and geology.
Xenotime is a rare-earth phosphate mineral, the major component of which is yttrium orthophosphate (YPO4). It forms a solid solution series with chernovite-(Y) (YAsO4) and therefore may contain trace impurities of arsenic, as well as silicon dioxide and calcium. The rare-earth elements dysprosium, erbium, terbium and ytterbium, as well as metal elements such as thorium and uranium (all replacing yttrium) are the expressive secondary components of xenotime. Due to uranium and thorium impurities, some xenotime specimens may be weakly to strongly radioactive. Lithiophyllite, monazite and purpurite are sometimes grouped with xenotime in the informal "anhydrous phosphates" group. Xenotime is used chiefly as a source of yttrium and heavy lanthanide metals (dysprosium, ytterbium, erbium and gadolinium). Occasionally, gemstones are also cut from the finest xenotime crystals.
Allanite (also called orthite) is a sorosilicate group of minerals within the broader epidote group that contain a significant amount of rare-earth elements. The mineral occurs mainly in metamorphosed clay-rich sediments and felsic igneous rocks. It has the general formula A2M3Si3O12[OH], where the A sites can contain large cations such as Ca2+, Sr2+, and rare-earth elements, and the M sites admit Al3+, Fe3+, Mn3+, Fe2+, or Mg2+ among others. However, a large amount of additional elements, including Th, U, Be, Zr, P, Ba, Cr and others may be present in the mineral. The International Mineralogical Association lists four minerals in the allanite group, each recognized as a unique mineral: allanite-(Ce), allanite-(La), allanite-(Nd), and allanite-(Y), depending on the dominant rare earth present: cerium, lanthanum, neodymium or yttrium.
Uranium–lead dating, abbreviated U–Pb dating, is one of the oldest and most refined of the radiometric dating schemes. It can be used to date rocks that formed and crystallised from about 1 million years to over 4.5 billion years ago with routine precisions in the 0.1–1 percent range.
Fission track dating is a radiometric dating technique based on analyses of the damage trails, or tracks, left by fission fragments in certain uranium-bearing minerals and glasses. Fission-track dating is a relatively simple method of radiometric dating that has made a significant impact on understanding the thermal history of continental crust, the timing of volcanic events, and the source and age of different archeological artifacts. The method involves using the number of fission events produced from the spontaneous decay of uranium-238 in common accessory minerals to date the time of rock cooling below closure temperature. Fission tracks are sensitive to heat, and therefore the technique is useful at unraveling the thermal evolution of rocks and minerals. Most current research using fission tracks is aimed at: a) understanding the evolution of mountain belts; b) determining the source or provenance of sediments; c) studying the thermal evolution of basins; d) determining the age of poorly dated strata; and e) dating and provenance determination of archeological artifacts.
Environmental radioactivity is produced by radioactive materials in the human environment. While some radioisotopes, such as strontium-90 (90Sr) and technetium-99 (99Tc), are only found on Earth as a result of human activity, and some, like potassium-40 (40K), are only present due to natural processes, a few isotopes, e.g. tritium (3H), result from both natural processes and human activities. The concentration and location of some natural isotopes, particularly uranium-238 (238U), can be affected by human activity.
Naturally occurring radioactive materials (NORM) and technologically enhanced naturally occurring radioactive materials (TENORM) consist of materials, usually industrial wastes or by-products enriched with radioactive elements found in the environment, such as uranium, thorium and potassium and any of their decay products, such as radium and radon. Produced water discharges and spills are a good example of entering NORMs into the surrounding environment.
The formation evaluation gamma ray log is a record of the variation with depth of the natural radioactivity of earth materials in a wellbore. Measurement of natural emission of gamma rays in oil and gas wells are useful because shales and sandstones typically have different gamma ray levels. Shales and clays are responsible for most natural radioactivity, so gamma ray log often is a good indicator of such rocks. In addition, the log is also used for correlation between wells, for depth correlation between open and cased holes, and for depth correlation between logging runs.
Cleusonite is a member of the crichtonite group of minerals with the chemical formula (Pb,Sr)(U4+
,U6+
)(Fe2+
,Zn)
2(Ti,Fe2+
,Fe3+
)
18(O,OH)
38. This group of minerals contains approximately thirteen complex metal titanates. The structures of minerals of this group is complicated by frequent fine-scale twinning and metamictization due to radioactive elements. The crichtonite group consists of members of related mineral species of the type A{BC2D6E12}O38 which are characterized by their predominant cations (as seen in crichtonite (Sr), senaite (Pb), davidite (REE + U), landauite (Na), loveringite (Ca), lindsleyite (Ba), and mathiasite (K).
Mineral alteration refers to the various natural processes that alter a mineral's chemical composition or crystallography.
Titanium in zircon geothermometry is a form of a geothermometry technique by which the crystallization temperature of a zircon crystal can be estimated by the amount of titanium atoms which can only be found in the crystal lattice. In zircon crystals, titanium is commonly incorporated, replacing similarly charged zirconium and silicon atoms. This process is relatively unaffected by pressure and highly temperature dependent, with the amount of titanium incorporated rising exponentially with temperature, making this an accurate geothermometry method. This measurement of titanium in zircons can be used to estimate the cooling temperatures of the crystal and infer conditions during which it crystallized. Compositional changes in the crystals growth rings can be used to estimate the thermodynamic history of the entire crystal. This method is useful as it can be combined with radiometric dating techniques that are commonly used with zircon crystals, to correlate quantitative temperature measurements with specific absolute ages. This technique can be used to estimate early Earth conditions, determine metamorphic facies, or to determine the source of detrital zircons, among other uses.
Rodney Charles Ewing is an American mineralogist and materials scientist whose research is focused on the properties of nuclear materials.