Osmium possesses quite remarkable chemical and physical properties. It has the highest melting point and the lowest vapor pressure in the platinum family. Osmium has a very low compressibility. Correspondingly, its bulk modulus is extremely high, reported between and , which rivals that of diamond (). However, the hardness of osmium is lower than diamond, only .
Osmium forms compounds with the oxidation states ranging from −2 to +8. The most common oxidation states are +2, +3, +4, and +8. The +8 oxidation state is notable for being the highest attained by any chemical element, and aside from osmium, is encountered only in xenon and ruthenium. The oxidation state −1 and −2 represented by the two reactive compounds and are used in the synthesis of osmium cluster compounds.
The most common compound exhibiting the +8 oxidation state is osmium tetroxide. This toxic compound is formed when powdered osmium is exposed to air, and is a very volatile, water-soluble, pale yellow, crystalline solid with a strong smell. Therefore, osmium powder has a characteristic smell of osmium tetroxide. Osmium tetroxide boils at 130 °C and is a powerful oxidizing agent. By contrast, osmium dioxide (OsO2) is black, non-volatile, and much less reactive and toxic.
Only two osmium compounds have major applications: osmium tetroxide — for staining tissue in electron microscopy and the non-volatile osmates for organic oxidation reactions.
In general, the lower oxidation states of osmium are stabilized by ligands that are good σ-donors (such as amines) and π-acceptors (heterocycles containing nitrogen). The higher oxidation states are stabilized by strong σ- and π-donors, such as and .
is the daughter of (half-life ) and is used extensively in dating terrestrial as well as meteoric rocks (see rhenium-osmium dating). It has also been used to measure the intensity of continental weathering over geologic time and to fix minimum ages for stabilization of the mantle roots of continental cratons. This decay is a reason why rhenium-rich minerals are abnormally rich in . However, the most notable application of Os in dating has been in conjunction with iridium, to analyze the layer of shocked quartz along the K-T boundary that marks the extinction of the dinosaurs 65 million years ago.
Uranium and osmium were early successful catalysts in the Haber process, the nitrogen fixation reaction of nitrogen and hydrogen to produce ammonia, giving enough yield to make the process economically successful. However, in 1908 cheaper catalysts based on iron and iron oxides were introduced for the first pilot plants.
Nowadays, osmium is primarily obtained from the processing of platinum and nickel ores.
Within the Earth's crust, osmium, like iridium, is found at highest concentrations in three types of geologic structure: igneous deposits (crustal intrusions from below), impact craters, and deposits reworked from one of the former structures. The largest known primary reserves are in the Bushveld igneous complex in South Africa, though the large copper–nickel deposits near Norilsk in Russia, and the Sudbury Basin in Canada are also significant sources of osmium. Smaller reserves can be found in the United States.
After it is dissolved, osmium is separated from the other platinum group metals by distillation or extraction with organic solvents of the volatile osmium tetroxide. The first method is similar to the procedure used by Tennant and Wollaston. Both methods are suitable for industrial scale production. In either case, the product is reduced using hydrogen, yielding the metal as a powder or sponge that can be treated using powder metallurgy techniques.
Neither the producers nor the United States Geological Survey published any production amounts for osmium. Estimations of the United States consumption date published from 1971, which gives a consumption in the United States of 2000 troy ounces (62 kg), would suggest that the production is still less than 1 ton per year.
Osmium tetroxide has been used in fingerprint detection and in staining fatty tissue for optical and electron microscopy. As a strong oxidant, it cross-links lipids mainly by reacting with unsaturated carbon-carbon bonds, and thereby both fixes biological membranes in place in tissue samples and simultaneously stains them. Because osmium atoms are extremely electron dense, osmium staining greatly enhances image contrast in transmission electron microscopy (TEM) studies of biological materials. Those carbon materials have otherwise very weak TEM contrast (see image). Another osmium compound, osmium ferricyanide (OsFeCN), exhibits similar fixing and staining action.
An alloy of 90% platinum and 10% osmium is used in surgical implants such as pacemakers and replacement of pulmonary valves.
The tetroxide and a related compound, potassium osmate, are important oxidants for chemical synthesis, despite being very poisonous. For the Sharpless asymmetric dihydroxylation, which uses osmate for the conversion of a double bond into a vicinal diol, Karl Barry Sharpless won the Nobel Prize in Chemistry in 2001.
In 1898 an Austrian chemist, Auer von Welsbach, developed the Oslamp with a filament made of osmium, which he introduced commercially in 1902. After only a few years, osmium was replaced by the more stable metal tungsten (also known as wolfram). Tungsten has the highest melting point of any metal, and using it in light bulbs increases the luminous efficacy and life of incandescent lamps.
Like palladium, powdered osmium effectively absorbs hydrogen atoms. This could make osmium a potential candidate for a metal hydride battery electrode. However, osmium is expensive and would react with potassium hydroxide, the most common battery electrolyte.
Osmium has high reflectivity in the ultraviolet range of the electromagnetic spectrum; for example, at 600 Å osmium has a reflectivity two times that of gold. This high reflectivity is desirable in space-based UV spectrometers which have reduced mirror sizes due to space limitations. Osmium-coated mirrors were flown in several space missions aboard the Space Shuttle, but it soon became clear that the oxygen radicals in the low earth orbit are abundant enough to significantly deteriorate the osmium layer.
Category:Chemical elements Category:Transition metals Category:Noble metals Category:Precious metals *
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