Yttrium is a chemical element; it has symbol Y and atomic number 39. It is a silvery-metallic transition metal chemically similar to the and has often been classified as a "rare-earth element". Yttrium is almost always found in combination with lanthanide elements in rare-earth minerals and is never found in nature as a free element. 89Y is the only stable isotope and the only isotope found in the Earth's crust.
The most important present-day use of yttrium is as a component of , especially those used in . Historically, it was once widely used in the red phosphors in television set cathode ray tube displays. Yttrium is also used in the production of , , electronic filters, , , various medical applications, and Trace element various materials to enhance their properties.
Yttrium has no known Biology role. Exposure to yttrium compounds can cause lung disease in humans.
The pure element is relatively stable in air in bulk form, due to passivation of a protective oxide () film that forms on the surface. This film can reach a thickness of 10 micrometre when yttrium is heated to 750 °Celsius in water vapor. When finely divided, however, yttrium is very unstable in air; shavings or swarf of the metal can ignite in air at temperatures exceeding 400 °C. Yttrium nitride (YN) is formed when the metal is heated to 1000 °C in nitrogen.
It often also falls in the same range for reaction order, resembling terbium and dysprosium in its chemical reactivity. Yttrium is so close in size to the so-called 'yttrium group' of heavy lanthanide ions that in solution, it behaves as if it were one of them. Even though the lanthanides are one row farther down the periodic table than yttrium, the similarity in atomic radius may be attributed to the lanthanide contraction.
One of the few notable differences between the chemistry of yttrium and that of the lanthanides is that yttrium is almost exclusively trivalent, whereas about half the lanthanides can have valences other than three; nevertheless, only for four of the fifteen lanthanides are these other valences important in aqueous solution (cerium, samarium, europium, and ytterbium).Daane 1968, p. 817
Yttrium forms a water-insoluble fluoride, hydroxide, and oxalate, but its bromide, chloride, iodide, nitrate and sulfate are all solubility in water. The Y ion is colorless in solution due to the absence of electrons in the d and f .
Water readily reacts with yttrium and its compounds to form . Concentrated nitric acid and hydrofluoric acids do not rapidly attack yttrium, but other strong acids do.
With , yttrium forms halide such as yttrium(III) fluoride (), yttrium(III) chloride (), and yttrium(III) bromide () at temperatures above roughly 200 °C. Similarly, carbon, phosphorus, selenium, silicon and sulfur all form with yttrium at elevated temperatures.
Organoyttrium chemistry is the study of compounds containing carbon–yttrium bonds. A few of these are known to have yttrium in the oxidation state 0. (The +2 state has been observed in chloride melts, and +1 in oxide clusters in the gas phase.) Some trimerization reactions were generated with organoyttrium compounds as catalysts. These syntheses use as a starting material, obtained from and concentrated hydrochloric acid and ammonium chloride.
Hapticity is a term to describe the coordination of a group of contiguous atoms of a ligand bound to the central atom; it is indicated by the Greek letter eta, η. Yttrium complexes were the first examples of complexes where carborane ligands were bound to a d-metal center through a η-hapticity. Vaporization of the graphite intercalation compounds graphite–Y or graphite– leads to the formation of endohedral fullerenes such as Y@C. Electron spin resonance studies indicated the formation of Y and (C) ion pairs. The YC, YC, and YC can be hydrolyzed to form .
Yttrium isotopes are among the most common products of the nuclear fission of uranium in nuclear explosions and nuclear reactors. In the context of nuclear waste management, the most important isotopes of yttrium are Y and Y, with half-lives of 58.51 days and 64 hours, respectively. Though Y has a short half-life, it exists in secular equilibrium with its long-lived parent isotope, strontium-90 (Sr) (half-life 29 years).
All group 3 elements have an odd atomic number, and therefore few stable . Scandium has one stable isotope, and yttrium itself has only one stable isotope, Y, which is also the only isotope that occurs naturally. However, the lanthanide rare earths contain elements of even atomic number and many stable isotopes. Yttrium-89 is thought to be more abundant than it otherwise would be, due in part to the s-process, which allows enough time for isotopes created by other processes to decay by beta decay (neutron → proton).
Such a slow process tends to favor isotopes with atomic mass numbers (A = protons + neutrons) around 90, 138 and 208, which have unusually stable atomic nucleus with 50, 82, and 126 neutrons, respectively. This stability is thought to result from their very low neutron-capture cross-section. Electron emission of isotopes with those mass numbers is simply less prevalent due to this stability, resulting in them having a higher abundance.
At least 32 synthetic isotopes of yttrium have been observed, and these range in atomic mass number from 76 to 108. The least stable of these is Y with a half-life of 25 SI prefix and the most stable is Y with half-life 106.629 days. Apart from Y, Y, and Y, with half-lives of 58.51 days, 79.8 hours, and 64 hours, respectively; all other isotopes have half-lives of less than a day and most of less than an hour.
Yttrium isotopes with mass numbers at or below 88 decay mainly by positron emission (proton → neutron) to form strontium (atomic number = 38) isotopes. Yttrium isotopes with mass numbers at or above 90 decay mainly by electron emission (neutron → proton) to form zirconium (Z = 40) isotopes. Isotopes with mass numbers at or above 97 are also known to have minor decay paths of β delayed neutron emission.
Yttrium has at least 20 metastable ("excited") isomers ranging in mass number from 78 to 102. Multiple excitation states have been observed for Y and Y. While most yttrium isomers are expected to be less stable than their ground state; Y have longer half-lives than their ground states, as these isomers decay by beta decay rather than isomeric transition.
Johan Gadolin at the Royal Academy of Åbo (Turku) identified a new oxide (or "earth") in Arrhenius' sample in 1789, and published his completed analysis in 1794.Gadolin 1794 Anders Gustaf Ekeberg confirmed the identification in 1797 and named the new oxide yttria. In the decades after Antoine Lavoisier developed the first modern definition of , it was believed that earths could be reduced to their elements, meaning that the discovery of a new earth was equivalent to the discovery of the element within, which in this case would have been yttrium.
Friedrich Wöhler is credited with first isolating the metal in 1828 by reacting a volatile chloride that he believed to be yttrium chloride with potassium.Heiserman, David L. (1992). "Element 39: Yttrium". Exploring Chemical Elements and their Compounds. New York: TAB Books. pp. 150–152. .
In 1843, Carl Gustaf Mosander found that samples of yttria contained three oxides: white yttrium oxide (yttria), yellow terbium oxide (confusingly, this was called 'erbia' at the time) and rose-colored erbium oxide (called 'terbia' at the time). A fourth oxide, ytterbium oxide, was isolated in 1878 by Jean Charles Galissard de Marignac. New elements were later isolated from each of those oxides, and each element was named, in some fashion, after Ytterby, the village near the quarry where they were found (see ytterbium, terbium, and erbium). In the following decades, seven other new metals were discovered in "Gadolin's yttria". Since yttria was found to be a mineral and not an oxide, Martin Heinrich Klaproth renamed it gadolinite in honor of Gadolin.
Until the early 1920s, the chemical symbol Yt was used for the element, after which Y came into common use.
In 1987, yttrium barium copper oxide was found to achieve high-temperature superconductivity. It was only the second material known to exhibit this property, and it was the first-known material to achieve superconductivity above the (economically important) boiling point of nitrogen.
Yttrium is not considered a "bone-seeker" like strontium and lead. Normally, as little as is found in the entire human body; human breast milk contains 4 ppm. Yttrium can be found in edible plants in concentrations between 20 ppm and 100 ppm (fresh weight), with cabbage having the largest amount. With as much as 700 ppm, the seeds of woody plants have the highest known concentrations.
there are reports of the discovery of very large reserves of rare-earth elements in the deep seabed several hundred kilometers from the tiny Japanese island of Minami-Torishima Island, also known as Marcus Island. This location is described as having "tremendous potential" for rare-earth elements and yttrium (REY), according to a study published in ''Scientific Reports''. "This REY-rich mud has great potential as a rare-earth metal resource because of the enormous amount available and its advantageous mineralogical features," the study reads. The study shows that more than of rare-earth elements could be "exploited in the near future." As well as yttrium (Y), which is used in products like camera lenses and mobile phone screens, the rare-earth elements found are europium (Eu), terbium (Tb), and dysprosium (Dy).
Rare-earth elements (REEs) come mainly from four sources:
One method for obtaining pure yttrium from the mixed oxide ores is to dissolve the oxide in sulfuric acid and fractionate it by ion exchange chromatography. With the addition of oxalic acid, the yttrium oxalate precipitates. The oxalate is converted into the oxide by heating under oxygen. By reacting the resulting yttrium oxide with hydrogen fluoride, yttrium fluoride is obtained. When quaternary ammonium salts are used as extractants, most yttrium will remain in the aqueous phase. When the counter-ion is nitrate, the light lanthanides are removed, and when the counter-ion is thiocyanate, the heavy lanthanides are removed. In this way, yttrium salts of 99.999% purity are obtained. In the usual situation, where yttrium is in a mixture that is two-thirds heavy-lanthanide, yttrium should be removed as soon as possible to facilitate the separation of the remaining elements.
Annual world production of yttrium oxide had reached by 2001; by 2014 it had increased to . Global reserves of yttrium oxide were estimated in 2014 to be more than . The leading countries for these reserves included Australia, Brazil, China, India, and the United States. Only a few tonnes of yttrium metal are produced each year by reducing yttrium fluoride to a metal sponge with calcium magnesium alloy. The temperature of an arc furnace, in excess of 1,600 °C, is sufficient to melt the yttrium.
Yttria is used as a sintering additive in the production of porous silicon nitride.
Yttrium compounds are used as a catalyst for ethylene polymerization. As a metal, yttrium is used on the electrodes of some high-performance spark plugs. Yttrium is used in for propane as a replacement for thorium, which is radioactive.
YAG, yttria, yttrium lithium fluoride (LiYF), and yttrium orthovanadate (YVO) are used in combination with such as neodymium, erbium, ytterbium in near-infrared . YAG lasers can operate at high power and are used for drilling and cutting metal. The single crystals of doped YAG are normally produced by the Czochralski process.
Yttrium can be used to Deoxidizer vanadium and other non-ferrous metals. Yttria stabilizes the cubic zirconia in jewelry.
Yttrium has been studied as a nodulizer in ductile cast iron, forming the graphite into compact nodules instead of flakes to increase ductility and fatigue resistance. Having a high melting point, yttrium oxide is used in some ceramic and glass to impart shock resistance and low thermal expansion properties. Those same properties make such glass useful in .
A technique called radioembolization is used to treat hepatocellular carcinoma and liver metastasis. Radioembolization is a low toxicity, targeted liver cancer therapy that uses millions of tiny beads made of glass or resin containing Y. The radioactive microspheres are delivered directly to the blood vessels feeding specific liver tumors/segments or lobes. It is minimally invasive and patients can usually be discharged after a few hours. This procedure may not eliminate all tumors throughout the entire liver, but works on one segment or one lobe at a time and may require multiple procedures.
Also see radioembolization in the case of combined cirrhosis and hepatocellular carcinoma.
Needles made of Y, which can cut more precisely than scalpels, have been used to sever pain-transmitting in the spinal cord, and Y is also used to carry out radionuclide synovectomy in the treatment of inflamed joints, especially knees, in people with conditions such as rheumatoid arthritis.
A neodymium-doped yttrium–aluminium–garnet laser has been used in an experimental, robot-assisted radical prostatectomy in canines in an attempt to reduce collateral nerve and tissue damage, and erbium-doped lasers are coming into use for cosmetic skin resurfacing.
The actual superconducting material is often written as YBa2Cu3O7– d, where d must be less than 0.7 for superconductivity. The reason for this is still not clear, but it is known that the vacancies occur only in certain places in the crystal, the copper oxide planes, and chains, giving rise to a peculiar oxidation state of the copper atoms, which somehow leads to the superconducting behavior.
The theory of low temperature superconductivity has been well understood since the BCS theory of 1957. It is based on a peculiarity of the interaction between two electrons in a crystal lattice. However, the BCS theory does not explain high temperature superconductivity, and its precise mechanism is still a mystery. What is known is that the composition of the copper-oxide materials must be precisely controlled for superconductivity to occur.
This superconductor is a black and green, multi-crystal, multi-phase mineral. Researchers are studying a class of materials known as that are alternative combinations of these elements, hoping to develop a practical high-temperature superconductor.
Exposure to yttrium compounds in humans may cause lung disease. Workers exposed to airborne yttrium europium vanadate dust experienced mild eye, skin, and upper respiratory tract irritation—though this may be caused by the vanadium content rather than the yttrium. Acute exposure to yttrium compounds can cause shortness of breath, coughing, chest pain, and cyanosis. The Occupational Safety and Health Administration (OSHA) limits exposure to yttrium in the workplace to over an 8-hour workday. The National Institute for Occupational Safety and Health (NIOSH) recommended exposure limit (REL) is over an 8-hour workday. At levels of , yttrium is IDLH. Yttrium dust is highly flammable.
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