Uranium (U)

Pure uranium is a silvery white, weakly radioactive metal, which is harder than most elements. It is malleable, ductile, slightly paramagnetic, strongly electropositive and is a poor electrical conductor. Uranium metal has very high density, being approximately 70% denser than lead, but slightly less dense than gold. Uranium metal exhibits in three crystallographic modifications: alpha > (688°C) > beta > (776°C) > gamma. Uranium is pyrophoric when finely divided. It is a little softer than steel and is attacked by cold water in a finely divided state.In air, uranium metal becomes coated with a layer of oxide. Acids dissolve the metal, forming the +3 oxidation state which oxidizes rapidly by water and air to form higher oxidation states. Uranium metal is unaffected by alkalis. Uranium metal can be prepared by reducing uranium halides with alkali or alkaline earth metals or by reducing uranium oxides by calcium, aluminum, or carbon at high temperatures. The metal can also be produced by electrolysis of KUF5 or UF4, dissolved in a molten salt mixture of CaCl2 and NaCl. High-purity uranium can be prepared by the thermal decomposition of uranium halides on a hot filament.

Uranium metal reacts with almost all nonmetallic elements and their compounds, with reactivity increasing with temperature. Hydrochloric and nitric acids dissolve uranium, but non-oxidizing acids other than hydrochloric acid attack the element very slowly. When finely divided, it can react with cold water. In air, uranium metal oxidizes and becomes coated with a dark layer of uranium oxide. Uranium forms a variety of alloys and compounds with the most important oxidation states being uranium(IV) and uranium(VI), and their two corresponding oxides are, respectively, uranium dioxide, UO2 and uranium trioxide, UO3. Besides the oxides, other Important uranium compounds include fluorides, chlorides, bromides, iodides, carbonates, hydrides, carbides, nitrides, phosphates, etc. At room temperatures, uranium hexafluoride, UF6, has a high vapor pressure, making it useful in the gaseous diffusion process used to separate the rare U-235 from the common U-238 isotope. Uranium hydrides, nitrides and carbides are relatively inertsemimetallic compounds that are minimally soluble in acids and have been used as stable fuel pellets in nuclear power reactor technology.

Uranium exists in aqueous solutions in the +3, +4, +5, and +6 oxidation states. Oxidation state +6 as the UO22+ ion (yellow in color) is the most stable state in solution. Uranium in the +5 state as the UO2+ ion is colorless, quite unstable and disproportionates (reacts with itself) to form the +6 and +4 states. The +4 state (green) is reasonably stable in solution, but the +3 state (dark green or dark red depending on the illumination source - daylight vs fluorescent light) is unstable and easily oxidizes to +4. The +4 state in near-neutral pH solutions readily hydrolyzes to form black oxy-hydroxide precipitates.

The name derives from the planet Uranus, which in Roman mythology was "Father Heaven". The German chemist Martin-Heinrich Klaproth discovered the element in 1789, following William Hershel's discovery of the planet in 1781. The metallic uranium was first isolated by the French chemist Eugène-Melchior Peligot in 1841.

Uranium was discovered by Martin Heinrich Klaproth, a German chemist, in the mineral pitchblende (primarily a mix of uranium oxides) in 1789. Although Klaproth, as well as the rest of the scientific community, believed that the substance he extracted from pitchblende was pure uranium, it was actually uranium dioxide (UO2). After noticing that 'pure' uranium reacted oddly with uranium tetrachloride (UCl4), Eugène-Melchoir Péligot, a French chemist isolated pure uranium by heating uranium dioxide with potassium in a platinum crucible. Radioactivity was first discovered in 1896 when Antoine Henri Becquerel, a French physicist, detected it from a sample of uranium. Today, uranium is obtained from uranium ores such as pitchblende, uraninite (UO2), carnotite (K2(UO2)2VO4·1-3H2O) and autunite (Ca(UO2)2(PO4)2·10H2O) as well as from phosphate rock (Ca3(PO4)2), lignite (brown coal) and monazite sand ((Ce, La, Th, Nd, Y)PO4). Since there is little demand for uranium metal, uranium is usually sold in the form of sodium diuranate (Na2U2O7·6H2O), also known as yellow cake, or triuranium octoxide (U3O8).

The use of uranium in its natural oxide form dates back to 79 A.D. when it was used as a yellow coloring agent in ceramic glazes. Yellow glass with 1% uranium oxide was found in an ancient Roman villa near Naples, Italy. In the late Middle Ages, pitchblende was extracted from the silver mines and was used as a coloring agent in the glassmaking industry. The identification of uranium as an element is generally credited to Martin H. Klaproth. While experimenting with pitchblende in 1789, he concluded that it contained a new element, which he named after the newly discovered planet Uranus (named after the Greek god of the sky or heaven). What Klaproth actually identified was not the pure element but uranium oxide. The pure metal was first isolated in 1841 by Eugène-Melchior Péligot, who reduced anhydrous uranium tetrachloride with potassium metal.

In 1896 Antoine H. Becquerel discovered that uranium exhibited invisible light or rays; it was radioactivity. In 1934 research by Enrico Fermi and others eventually led to the use of uranium fission in the first nuclear weapon used in war and later in the peaceful use of uranium as fuel in nuclear power production. An ensuing arms race during the Cold War between the United States and the Soviet Union produced tens of thousands of nuclear weapons that used uranium metal and uranium-derived plutonium-239. The security of those weapons and their fissile material following the breakup of the Soviet Union in 1991 is an ongoing concern.

In 1972 French physicist Francis Perrin discovered ancient and no longer active prehistoric natural nuclear fission reactors in uranium ore deposits at the Oklo mine in Gabon, West Africa, collectively known as the Oklo Fossil Reactors. The ore deposit is 1.7 billion years old; at that time, uranium-235 constituted about 3% of the total uranium on Earth (0.72% today). This is high enough to permit a sustained nuclear fission chain reaction to occur, provided other supporting geologic conditions exist.