TERBIUM Chemical Properties
- Melting point:
- 1356 °C(lit.)
- Boiling point:
- 3230 °C(lit.)
- 8.234 g/mL at 25 °C(lit.)
- Specific Gravity
- 116 μΩ-cm, 20°C
- Water Solubility
- Insoluble in water.
- Air & Moisture Sensitive
- Stable, but moisture sensitive. Reacts with halogens, strong acids. The powder is highly flammable.
- CAS DataBase Reference
- 7440-27-9(CAS DataBase Reference)
- EPA Substance Registry System
- Terbium (7440-27-9)
TERBIUM Usage And Synthesis
Terbium is primarily used in phosphors, particularly in fluorescent lamps and as the high intensity green emitter used in projection televisions, such as the Yttrium-Aluminum-Garnet (Tb:YAG) variety.
Terbium responds efficiently to x-ray excitation and is, therefore, used as an x-ray phosphor.
Terbium compounds are useful biological probes due to the long emission lifetime of terbium.
Terbium alloys are also used in magneto-optic recording films, such as TbFeCo.
Terbium is also used in alloys and in the production of electronic devices. As a component of Terfenol-D, Terbium is of use in actuators, in naval sonar systems, sensors, in the SoundBug device (its first commercial application), and other magnetomechanical devices.
Terbium Metal is the important additive for NdFeB permanent magnets to raise the Curie temperature and improve temperature coefficiency. Another most promising use of distilled Terbium Metal, code 6563D, is in the magnetostrictive alloy TEFENOL-D. There are also other applications for some special master alloys. Terbium Metal can be further processed to various shapes of ingots, pieces, wires, foils, slabs, rods, discs and powder.
silvery-white chip or ingot, or grey powder
There are two allotropic (crystal forms) of terbium, both of which are dependent on itstemperature. The alpha ((α) form exists at room temperatures and up to temperatures of1,298°C, and the beta (β) form exists beyond these temperatures. Although terbium is a silverymetal that resembles aluminum and feels like lead, it is much heavier than either of thesetwo elements. It is placed in the yttrium subgroup (lanthanide series) of the rare-earths. It isalso resistant to corrosion.
Its melting point is 1,356.9°C, its boiling point is 3,230°C, and its density is 8.23g/cm3.
There are a total of 52 isotopes of terbium, and only one of these is stable (Tb-159). Terbium-59 makes up 100% of the element found in the Earth’s crust.
Origin of Name
Named for a village in Sweden.
Of all the 17 rare-earths in the lanthanide series, terbium is number 14 in abundance.Terbium can be separated from the minerals xenotime (YPO4) and euxenite, a mixture of thefollowing: (Y, Ca, Er, La, Ce, Y, Th)(Nb, Ta, Ti2O6). It is obtained in commercial amountfrom monazite sand by the ion-exchange process. Monazite may contain as much as 50%rare-earth elements, and about 0.03% of this is terbium.
Terbium is not found in great quantities on Earth. In fact, minerals where terbium is foundcontain about 0.03% terbium. Not much of the stable isotope is found as a free metal; rathermost of it is mixed with other rare-earths or are in compound forms.
Discovered by Mosander in 1843. Terbium is a member of the lanthanide or “rare earth” group of elements. It is found in cerite, gadolinite, and other minerals along with other rare earths. It is recovered commercially from monazite in which it is present to the extent of 0.03%, from xenotime, and from euxenite, a complex oxide containing 1% or more of terbia. Terbium has been isolated only in recent years with the development of ion-exchange techniques for separating the rareearth elements. As with other rare earths, it can be produced by reducing the anhydrous chloride or fluoride with calcium metal in a tantalum crucible. Calcium and tantalum impurities can be removed by vacuum remelting. Other methods of isolation are possible. Terbium is reasonably stable in air. It is a silver-gray metal, and is malleable, ductile, and soft enough to be cut with a knife. Two crystal modifications exist, with a transformation temperature of 1289°C. Forty-two isotopes and isomers are recognized. The oxide is a chocolate or dark maroon color. Sodium terbium borate is used as a laser material and emits coherent light at 0.546 μm. Terbium is used to dope calcium fluoride, calcium tungstate, and strontium molybdate, used in solid-state devices. The oxide has potential application as an activator for green phosphors used in color TV tubes. It can be used with ZrO2 as a crystal stabilizer of fuel cells that operate at elevated temperature. Few other uses have been found. The element is priced at about $40/g (99.9%). Little is known of the toxicity of terbium. It should be handled with care as with other lanthanide elements.
Phosphor activator, dope for solid-state devices.
There are few uses for terbium. However, terbium can be used as an activator for greenphosphor in TV tubes, and some of its compounds are used to produce laser lights. It is alsoused to “dope” (coat) some forms of solid-state instruments, as a stabilizer in fuel cells so thatthey can operate at high temperatures, and as a metal for control rods in nuclear reactors.
Atomic number 65, group IIIB of the periodic table, a rare-earth element of the yttrium subgroup (lanthanide series), aw 158.9254, valences of 3, 4; no stable isotopes.
A soft ductile malleable silvery rare element of the lanthanoid series of metals. It occurs in association with other lanthanoids. One of its few uses is as a dopant in solid-state devices. Symbol: Tb; m.p. 1356°C; b.p. 3123°C; r.d. 8.229 (20°C); p.n. 65; r.a.m. 158.92534.
terbium: Symbol Tb. A silverymetallic element belonging to thelanthanoids; a.n. 65; r.a.m. 158.92;r.d. 8.23 (20°C); m.p. 1356°C; b.p.3123°C. It occurs in apatite and xenotime,from which it is obtained by anion-exchange process. There is onlyone natural isotope, terbium–159,which is stable. Seventeen artificialisotopes have been identified. It isused as a dopant in semiconductingdevices. It was discovered by CarlMosander (1797–1858) in 1843.
Terbium is recovered from the minerals, monazite, xenotime, and euxenite. The recovery processes are quite similar to those of other lanthanide elements (See individual lanthanide elements). The metal is separated from other rareearths by ion exchange methods, which are relatively easy and faster than fractional crystallization techniques.
Terbium metal is obtained from its anhydrous trifluoride, TbF3, or trichloride, TbCl3, by thermal reduction with calcium, carried out in a tantalum crucible. Terbium produced by such methods may contain traces of calcium and tantalum. High purity metal can be prepared by various methods such as vacuum remelting, distillation, amalgam formation, floating zone melting, and various chemical processes.
The halogens (group VIIA) of terbium are strong irritants. Most of the compounds aretoxic and some are explosive. A vacuum or inert atmosphere must be maintained when workingwith the metal because of its strong oxidation properties.
- TERBIUM - TB4O7, 99.99%, 2% HNO3 500ML
- TERBIUM - 10% HCL 250ML
- TERBIUM PIECES, 99.9% (REO)
- TERBIUM FOIL, 0.25MM (0.01IN) THICK, 99.9% (REO)
- TERBIUM, STANDARD SOLUTION 1000 MG/L TB FOR ICP (TERBIUM OXIDE IN NITRIC ACID 2%)
- TERBIUM HYDROXIDE
- TERBIUM ARSENIDE
- TERBIUM PHOSPHIDE
- TERBIUM ACETATE
- Terbium(III) chloride
- Terbium(III) fluoride
- TERBIUM BISMUTHIDE
- TERBIUM ARSENATE
- terbium nitride
- TERBIUM ANTIMONIDE
- TERBIUM NITRATE, HEXAHYDRATE
- TERBIUM(III) SULFATE
- 400-666-7788 010-82848833-
- 400-660-8290 21-61259100-
- 010-57411838 010-57411839-
- 400-005-6266 021-58432009