Rhenium is a chemical element with symbol Re and atomic number 75. It is a silvery-white, heavy, third-row transition metal in group 7 of the periodic table. With an estimated average concentration of 1 part per billion (ppb), rhenium is one of the rarest elements in the Earth's crust.
Rhenium has a half-filled d-shell electron configuration ([Xe] 4f¹⁴ 5d⁵ 6s²). It is famous in inorganic chemistry for exhibiting the widest range of oxidation states of any known chemical element, spanning from −3 to +7, with the +7, +6 and +4 states being the most representative and stable. It is a very dense, silvery-white transition metal with intense metallic luster in group 7. It has the third highest melting point among the chemical elements (3,186 °C), surpassed only by tungsten and carbon, and notable resistance to mechanical deformation at extreme temperatures (creep resistance).
4 Re + 7 O₂ → 2 Re₂O₇
When heated in a stream of oxygen or air above 400 °C it burns to form volatile, bright-yellow rhenium heptoxide.
3 Re + 7 HNO₃ → 3 HReO₄ + 7 NO + 2 H₂O
It is not attacked by hydrochloric or hydrofluoric acid, but actively dissolves in oxidizing acids such as concentrated nitric acid to form transparent perrhenic acid.
Re₂O₇ + H₂O → 2 HReO₄
Rhenium heptoxide is highly hygroscopic and reacts vigorously with water to form perrhenic acid, a strong inorganic acid.
2 Re + 5 F₂ → 2 ReF₅
It combines directly with halogens to form various high-valence halides such as fluorides and chlorides in exothermic reactions.
| Compound | Formula | Use or importance |
|---|---|---|
| Rhenium heptoxide | Re₂O₇ | Highly volatile yellow crystalline solid; basic precursor for synthesizing rhenium compounds and catalysts |
| Ammonium perrhenate | NH₄ReO₄ | White crystalline salt; the industry standard for commercializing, transporting and refining rhenium worldwide |
| Methylrhenium trioxide | CH₃ReO₃ | Organometallic catalyst of extraordinary efficacy and selectivity in olefin epoxidation reactions |
| Rhenium(VII) sulfide | Re₂S₇ | Insoluble precursor used to prepare hydrogenation and desulfurization catalysts in the petroleum industry |
Natural rhenium is made up of two isotopes: rhenium-185 (¹⁸⁵Re), stable with 110 neutrons (37.40%), and rhenium-187 (¹⁸⁷Re), a primordial beta-emitting radionuclide with 112 neutrons that makes up most of the natural element (62.60%) despite being radioactive, thanks to its colossal half-life of 41.2 billion years. The decay of ¹⁸⁷Re into osmium-187 constitutes the rhenium–osmium geochronology system, used to date copper and gold sulfide ore deposits and study meteorite impacts on Earth.
It is one of the scarcest elements in the Earth's crust (with an estimated average concentration of only 1 part per billion or 1 ppb), ranking among the ten rarest elements on the planet. There are no primary rhenium mines; the only known ore of its own, rhenite (ReS₂), is a geological rarity that condenses in active volcanic fumaroles in the Kuril Islands. Rhenium is recovered exclusively on a commercial scale as a byproduct of roasting molybdenite (MoS₂) concentrates, which in turn come from copper porphyry mining, mainly in Chile, the United States, Poland and Peru.
It was the last non-radioactive natural chemical element to be discovered. Although in 1908 the Japanese chemist Masataka Ogawa detected a new element in thorianite, he mistakenly identified it as element 43; the definitive, formal discovery was achieved in 1925 by the German chemists Ida Noddack, Walter Noddack and Otto Berg in Berlin after analyzing columbite and platinum samples by X-ray spectroscopy. They named it 'rhenium' after the river Rhine (Rhenus in Latin) and the German region of Rhineland.
Over 70% of world rhenium production goes into making single-crystal nickel superalloys for blades and discs in the turbine engines of commercial and military aviation (Boeing, Airbus, fighter jets). Adding between 3% and 6% prevents the blades from deforming plastically ('creep') above 1,000 °C in the flow of combustion gases. It is also used in thermocouples to measure temperatures up to 2,200 °C and in filaments for mass spectrometers.
Rhenium forms platinum–rhenium (Pt-Re) bimetallic catalysts on alumina, vital in oil refinery catalytic reforming to produce high-octane unleaded gasolines. Methylrhenium trioxide (MTO) is a green selective catalyst in pharmaceutical synthesis.
It plays no known biological role in any living organism. Its natural concentrations are infinitesimal and the perrhenate ions (ReO₄⁻) show very low acute toxicity in laboratory biological tests, being excreted in urine without bioaccumulating in organs.
Metallic rhenium and its alloys are biologically and chemically stable, with no toxicological risks from contact or handling. Fine powders may pose a fire hazard when heated in an oxidizing atmosphere, and rhenium heptoxide vapors are acidic and irritating to the eyes.
Due to its extreme scarcity, its industrial use is subject to rigorous recycling of spent catalysts and aviation turbine scrap. Emissions to the environment are insignificant and no ecotoxic effects are recorded in freshwater or marine ecosystems.
Rhenium is incorporated into certain superalloys used in aircraft turbines because it helps maintain their mechanical strength at high temperatures. These parts endure intense heat and great stresses while the engine runs. Rhenium is scarce and expensive, so it is reserved for specialized alloys. Its presence can improve certain properties, although the design and cooling of the parts are also essential.
Rhenium-187 slowly decays by emitting beta particles to become osmium-187, with a half-life of 41.2 billion years. Unlike other geological clocks based on silicates, both rhenium and osmium are strongly siderophile and chalcophile, concentrating in sulfide minerals such as molybdenite. By measuring the ¹⁸⁷Re/¹⁸⁷Os ratio in sulfide crystals, geologists can determine with millimeter precision the exact date when the great copper and gold porphyry deposits precipitated.
In the catalytic reforming of oil refineries, heavy low-octane naphthas are converted into branched high-octane aromatic hydrocarbons for unleaded gasolines. Traditional pure-platinum catalysts deactivated quickly because carbon ('coke') deposited on the metal, blocking it. Alloying platinum with rhenium catalytically breaks up the coke precursors and prevents their buildup, allowing the reactor to run without interruption for years at high pressure and temperature.
Most temperature sensors melt or degrade above 1,700 °C. Thermocouples based on tungsten alloys with 5% rhenium paired with tungsten and 26% rhenium exploit the extremely high melting points of both refractory metals. Adding rhenium eliminates the mechanical brittleness typical of recrystallized tungsten, allowing millimeter-faithful measurement of infernal temperatures up to 2,300 °C in nuclear reactors and sintering furnaces.
Unlike other metals that form concentrated, visible minerals, rhenium is one of the scarcest elements in the Earth's crust (barely one part per billion). It also tends to hide, dispersed in microscopic amounts, inside molybdenum and platinum minerals. That is why chemists needed very advanced X-ray analysis techniques in 1925 to detect it for the first time.
Rhenite (ReS₂) was the first pure rhenium mineral confirmed on Earth, found at the Kudriavy volcano in the Kuril Islands. In the deep magma, volcanic gases above 900 °C carry rhenium in the gas phase. As they emerge to the surface through cracks and meet the cold air, rhenium sulfide vapor sublimes directly as fine metallic crystals on the walls of active fumaroles.
Rhenium-187 is radioactive, but its half-life is so long that only a small fraction decays on time scales comparable to the age of the Earth. That is why it remains the most abundant isotope of natural rhenium. It slowly turns into osmium-187, a property that geologists use to study the age and origin of certain rocks and minerals.
Main sources consulted: PubChem, Royal Society of Chemistry, NIST, IUPAC. Last revision: November 2026.