Generated by DeepSeek V3.2| dysprosium | |
|---|---|
| Name | dysprosium |
| Number | 66 |
| Category | lanthanide |
| Group | n/a |
| Appearance | silvery white |
| Standard atomic weight | 162.500(1) |
| Electron configuration | [Xe] 4f10 6s2 |
| Phase | solid |
| Density gpcm3 | 8.540 |
| Melting point K | 1680 |
| Boiling point K | 2840 |
dysprosium. It is a chemical element with the symbol Dy and atomic number 66. Classified as a lanthanide, it is a rare-earth metal with a bright, silvery luster. The element is relatively stable in air at room temperature but dissolves readily in mineral acids. Dysprosium possesses unique magnetic and thermal properties that make it critical for several advanced technological applications.
Dysprosium is a soft, malleable metal with a high melting point, similar to other members of the lanthanide series. It exhibits ferromagnetic ordering below 85 K, and its magnetic strength is exceptionally high, particularly at low temperatures. The element has a high neutron absorption cross-section, making it useful in nuclear control applications. Its most common oxidation state is +3, giving rise to compounds like dysprosium(III) oxide and dysprosium(III) chloride. The absorption spectrum of dysprosium ions shows sharp bands, which are characteristic of f-electron systems. At elevated temperatures, it can ignite and burn to form its oxide.
The element was first identified in 1886 by French chemist Paul-Émile Lecoq de Boisbaudran, who had previously discovered gallium and samarium. He detected its oxide, then known as dysprosia, through spectroscopic analysis of an erbia sample from the mineral gadolinite. The name derives from the Greek *dysprositos*, meaning "hard to get," reflecting the difficulty Boisbaudran experienced in isolating it. For decades, dysprosium remained a laboratory curiosity. It was not until the development of ion-exchange techniques in the mid-20th century, pioneered by scientists like Frank Spedding at the Ames Laboratory, that relatively pure metallic dysprosium could be produced.
Dysprosium is never found in nature as a free element. It occurs in several minerals, most notably xenotime, monazite, and bastnäsite, which are the primary commercial sources for all rare-earth elements. Significant deposits are mined in Bayan Obo in Inner Mongolia, at the Mountain Pass mine in California, and from the Mount Weld deposit in Australia. The extraction process is complex, involving crushing the ore, followed by various separation steps like froth flotation, leaching, and solvent extraction. Final purification to metallic form is achieved through metallothermic reduction, typically using calcium or lithium as a reducing agent under an inert argon atmosphere.
The primary use of dysprosium is in manufacturing high-strength neodymium-iron-boron magnets, where it is added to improve coercivity and performance at elevated temperatures, crucial for motors in electric vehicles and wind turbine generators. Its high neutron absorption cross-section makes it ideal for control rods in nuclear reactors, such as those in the CANDU reactor design. Dysprosium compounds are used in dosimeters for measuring ionizing radiation exposure. Furthermore, dysprosium cadmium chalcogenides are studied for their magnetocaloric effect. The element is also employed in dysprosium iodide lamps to produce an intense white light and in certain laser materials.
Dysprosium has no known biological role in any organism, including humans. Its compounds are generally regarded as having low to moderate toxicity, but details are not fully established. As a fine powder or dust, metallic dysprosium presents a fire and explosion hazard. Soluble dysprosium salts are considered slightly toxic if ingested, while insoluble compounds are mostly inert. In industrial settings, such as mining and magnet manufacturing, standard precautions for handling heavy metals and fine particulates should be observed to prevent inhalation or chronic exposure.
Category:Lanthanides Category:Chemical elements