Lanthanide
Terbium is a chemical element; it has symbol Tb and atomic number 65. It is a silvery-white, rare earth metal that is malleable and ductile. The ninth member of the lanthanide series, terbium is a fairly electropositive metal that reacts with water, evolving hydrogen gas. Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite, xenotime and euxenite.
Swedish chemist Carl Gustaf Mosander discovered terbium as a chemical element in 1843. He detected it as an impurity in yttrium oxide (Y2O3). Yttrium and terbium, as well as erbium and ytterbium, are named after the village of Ytterby in Sweden. Terbium was not isolated in pure form until the advent of ion exchange techniques.
Terbium is used to dope calcium fluoride, calcium tungstate and strontium molybdate in solid-state devices, and as a crystal stabilizer of fuel cells that operate at elevated temperatures. As a component of Terfenol-D (an alloy that expands and contracts when exposed to magnetic fields more than any other alloy), terbium is of use in actuators, in naval sonar systems and in sensors. Terbium is considered non-hazardous, though its biological role and toxicity have not been researched in depth.
Most of the world's terbium supply is used in green phosphors. Terbium oxide is used in fluorescent lamps and television and monitor cathode-ray tubes (CRTs). …
Swedish chemist Carl Gustaf Mosander discovered terbium in 1843. He detected it as an impurity in yttrium oxide, Y2O3, then known as yttria. Yttrium, erbium, and terbium are all named after the village of Ytterby in Sweden. Terbium was not isolated in pure form until the advent of ion exchange techniques.
Mosander first separated yttria into three fractions, all named for the ore: yttria, erbia, and terbia. "Terbia" was originally the fraction that contained the pink color, due to the element now known as erbium. "Erbia", the oxide containing what is now known as terbium, originally was the fraction that was yellow or dark orange in solution. The insoluble oxide of this element was noted to be tinged brown, and soluble oxides after combustion were noted to be colorless. Until the advent of spectral analysis, arguments went back and forth as to whether erbia even existed. Spectral analysis by Marc Delafontaine allowed the separate elements and their oxides to be identified, but in his publications, the names of erbium and terbium were switched, following a brief period where terbium was renamed "mosandrum", after Mosander. The names have remained switched ever since.
The early years of preparing terbium (as terbium oxide) were difficult. Metal oxides from gadolinite and samarskite were dissolved in nitric acid, and the solution was further separated using oxalic acid and potassium sulfate. …
Terbium is a silvery-white rare earth metal that is malleable, ductile and soft enough to be cut with a knife. It is relatively stable in air compared to the more reactive lanthanides in the first half of the lanthanide series. Terbium exists in two crystal allotropes with a transformation temperature of 1289 °C between them. The 65 electrons of a terbium atom are arranged in the electron configuration [Xe]4f96s2. The eleven 4f and 6s electrons are valence. Only three electrons can be removed before the nuclear charge becomes too great to allow further ionization, but in the case of terbium, the stability of the half-filled [Xe]4f7 configuration allows further ionization of a fourth electron in the presence of very strong oxidizing agents such as fluorine gas.
The terbium(III) cation (Tb3+) is brilliantly fluorescent, in a bright lemon-yellow color that is the result of a strong green emission line in combination with other lines in the orange and red. The yttrofluorite variety of the mineral fluorite owes its creamy-yellow fluorescence in part to terbium. Terbium easily oxidizes, and is therefore used in its elemental form specifically for research. Single terbium atoms have been isolated by implanting them into fullerene molecules. Trivalent europium (Eu3+) and Tb3+ ions are among the lanthanide ions that have garnered the most attention because of their strong luminosity and great color purity.
Terbium has a simple ferromagnetic ordering at temperatures below 219 K. …
Terbium occurs with other rare earth elements in many minerals, including monazite ((Ce,La,Th,Nd,Y)PO4 with up to 0.03% terbium), xenotime (YPO4) and euxenite ((Y,Ca,Er,La,Ce,U,Th)(Nb,Ta,Ti)2O6 with 1% or more terbium). The crust abundance of terbium is estimated as 1.2 mg/kg. No terbium-dominant mineral has yet been found.
Terbium (as the species Tb II) has been detected in the atmosphere of KELT-9b, a hot-Jupiter planet outside the Solar System.
Currently, the richest commercial sources of terbium are the ion-adsorption clays of southern China; the concentrates with about two-thirds yttrium oxide by weight have about 1% terbia. Small amounts of terbium occur in bastnäsite and monazite; when these are processed by solvent extraction to recover the valuable heavy lanthanides as samarium-europium-gadolinium concentrate, terbium is recovered therein. Due to the large volumes of bastnäsite processed relative to the ion-adsorption clays, a significant proportion of the world's terbium supply comes from bastnäsite.
In 2018, a rich terbium supply was discovered off the coast of Japan's Minamitori Island, with the stated supply being "enough to meet the global demand for 420 years".
Terbium is used as a dopant in calcium fluoride, calcium tungstate, and strontium molybdate, materials that are used in solid-state devices, and as a crystal stabilizer of fuel cells which operate at elevated temperatures, together with zirconium dioxide (ZrO2).
Terbium is also used in alloys and in the production of electronic devices. As a component of Terfenol-D, terbium is used in actuators, in naval sonar systems, sensors, and other magnetomechanical devices. Terfenol-D is a terbium alloy that expands or contracts in the presence of a magnetic field. It has the highest magnetostriction of any alloy. It is used to increase verdet constant in long-distance fiber optic communication. Terbium-doped garnets are also used in optical isolators, which prevents reflected light from traveling back along the optical fiber.
Terbium oxides are used in green phosphors in fluorescent lamps, color TV tubes, and flat screen monitors. Terbium, along with all other lanthanides except lanthanum and lutetium, is luminescent in the 3+ oxidation state. The brilliant fluorescence allows terbium to be used as a probe in biochemistry, where it somewhat resembles calcium in its behavior. Terbium "green" phosphors (which fluoresce a brilliant lemon-yellow) are combined with divalent europium blue phosphors and trivalent europium red phosphors to provide trichromatic lighting, which is by far the largest consumer of the world's terbium supply. …
Naturally occurring terbium is composed of its only stable isotope, terbium-159; the element is thus mononuclidic and monoisotopic. Thirty-nine radioisotopes have been characterized from 135Tb to 174Tb. The most stable synthetic radioisotopes of terbium are 158Tb, with a half-life of 180 years, and 157Tb, with a half-life of 71 years. All of the remaining radioactive isotopes have half-lives that are less than three months, and the majority of these have half-lives that are less than half a minute. The primary decay mode before the most abundant stable isotope, 159Tb, is electron capture, which results in production of gadolinium isotopes, and the primary mode after is beta minus decay, resulting in dysprosium isotopes.
The element also has 31 nuclear isomers, with masses of 141–154, 156, 158, 162, and 164–168 (not every mass number corresponds to only one isomer). The most stable of them are terbium-156m2, with a half-life of 24.4 hours, and terbium-154m2, with a half-life of 22.7 hours; this is more stable than ground states of terbium isotopes, except outside the mass range 155–161.
Terbium-149, with its half-life of 4.1 hours, is a promising candidate in targeted alpha therapy and positron emission tomography.
Terbium, along with many of the other rare earth elements, is poorly studied in terms of its toxicology and environmental impacts. Few health-based guidance values for safe exposure to terbium are available. No values are established in the United States by the Occupational Safety and Health Administration or American Conference of Governmental Industrial Hygienists at which terbium exposure becomes hazardous, and it is not considered a hazardous substance under the Globally Harmonized System of Classification and Labelling of Chemicals.
Reviews of the toxicity of the rare earth elements place terbium and its compounds as "of low to moderately toxicity", remarking on the lack of detailed studies on their hazards and the lack of market demand forestalling evidence of toxicity.
Some studies demonstrate environmental accumulation of terbium as hazardous to fish and plants. High exposures of terbium may enhance the toxicity of other substances causing endocytosis in plant cells.