Element 42 · transition metal
Molybdenum (Mo)
Almost all the nitrogen in your body was pulled out of the air by an enzyme with molybdenum at its centre. Atmospheric nitrogen is two atoms held together by a triple bond that industrial chemistry can only break at 400 °C and 200 atmospheres, and nitrogenase does it in soil at ambient temperature using an iron-molybdenum cofactor of seven iron atoms, nine sulfurs, a carbon and one molybdenum. No other second-row transition metal has anything like this significance to living things, and it makes molybdenum the outlier of its neighbourhood: ruthenium, niobium and zirconium are biologically inert, while the metal between them runs the nitrogen cycle.
A name that means lead
Molybdenite is soft, grey, greasy to the touch and leaves a mark on paper. So do graphite and galena, and for most of recorded history nobody distinguished them. All three went by the Greek word molybdos, lead, or its derivative molybdaina, and all three were sold as writing and marking materials. The confusion is preserved in a modern name too: what the English call a lead pencil has never contained any lead, because the graphite in it was another of the molybdenas.
Carl Wilhelm Scheele took the confusion apart in 1778, showing that the greasy mineral was neither graphite nor a lead ore but contained an unfamiliar metal. He could not reduce it himself and passed the problem to Peter Jacob Hjelm, who produced the metal in 1781 by heating the oxide with carbon in linseed oil. The conventional credit above names Scheele; the metal existed because of Hjelm.
A molybdenum famine in the ancient ocean
Molybdenum's biological role has an awkward geochemical consequence. The element dissolves in seawater only when conditions are oxidising, as the molybdate ion; in anoxic, sulfidic water it precipitates out as a sulfide and is buried in the sediment.
For the first half of Earth's history the ocean was anoxic and the deep water sulfidic, so dissolved molybdenum was scarce — and organisms that needed it to fix nitrogen were starved of it. Ariel Anbar and Andrew Knoll proposed this as a limit on early life: not a shortage of nitrogen, but a shortage of the metal required to access it, holding back eukaryotes for hundreds of millions of years until the oceans oxygenated enough to keep molybdenum in solution.
The evidence comes from molybdenum's own isotopes. The ratio of molybdenum-98 to molybdenum-95 in a sediment shifts depending on how oxidising the water above it was, because oxide surfaces preferentially adsorb the lighter isotope. Black shales of different ages therefore preserve a record of ocean oxygenation, and the molybdenum isotope curve is now one of the standard proxies for reconstructing the Great Oxidation Event and the sluggish, uneven rise of oxygen that followed it.
Why marine-grade stainless is marine-grade
Roughly four-fifths of the molybdenum mined ends up in steel, and its single most visible effect is corrosion resistance in the presence of chloride.
Ordinary 304 stainless steel is protected by a passive chromium oxide film. Chloride ions attack that film locally, and once a pit starts it becomes self-sustaining: the chemistry inside the pit turns acidic and the surface never repassivates. Adding two to three per cent molybdenum, which is the difference between 304 and 316, greatly raises the chloride concentration and temperature at which pitting begins. That is why 316 is specified for boat fittings, coastal architecture, swimming pool hardware, food processing and pharmaceutical plant, and why higher-molybdenum grades such as 6% Mo super-austenitics are used for seawater piping and desalination.
Molybdenum earns its place in other steels for a different reason. It raises hardenability, resists tempering, and suppresses creep — the slow deformation of metal held under load at high temperature. Chrome-moly steels are the standard for boiler tubes, pressure vessels and pipework in fossil and nuclear plant for exactly that reason, and high-speed tool steels rely on it to keep a cutting edge hot.
Its reputation in armour and artillery dates from the First World War, when molybdenum steel allowed lighter gun barrels and tougher plate. The Climax deposit in Colorado, until then a curiosity, was developed to meet that demand and became the largest molybdenum mine in the world.
Slippery where graphite fails
Molybdenum disulfide has the same kind of layered structure as graphite: strongly bonded sheets held together only weakly, so the sheets slide over each other. It is a very good dry lubricant for the same reason.
What makes it more than a graphite substitute is where it works. Graphite's lubricity depends on adsorbed water vapour between the layers, so it fails in vacuum — a genuine problem for spacecraft mechanisms, which is how the difference was discovered. Molybdenum disulfide needs no adsorbed film and keeps working in vacuum and at temperatures where oils carbonise. It goes into greases, bonded coatings for threaded fasteners, and the sliding surfaces of satellite hardware.
The same layered material has a second life in research: a single molecular sheet of molybdenum disulfide is a two-dimensional semiconductor with a genuine band gap, which is the property graphene lacks, and it has become one of the most studied materials in nanoelectronics.
The atom nobody uses as molybdenum
Molybdenum-99 is worth more per gram than anything else the element produces, and it is not wanted for any chemical purpose. It is made by fissioning uranium targets in a research reactor, or by neutron activation of molybdenum-98, and it is valuable purely because of what it turns into: the short-lived nuclear isomer used in the majority of the world's diagnostic imaging. The parent is shipped; the daughter is what gets injected. A reactor irradiation lasting days feeds a distribution network that has to work to the clock.
Half of it is a byproduct of copper
Molybdenite is the only ore that matters, and it comes from two very different kinds of operation. Primary mines — Climax and Henderson in Colorado, and several in China — are worked for molybdenum alone. The other roughly half of world supply is recovered from the flotation circuits of porphyry copper mines in Chile, Peru, the United States and Mexico, where molybdenite is separated from the copper concentrate almost as an afterthought.
That split gives molybdenum an unusual price behaviour. When copper output is high the byproduct supply arrives regardless of what molybdenum is worth, which caps prices; when demand for alloy steels spikes, only the primary mines can respond, and they take time to restart. The result is one of the more volatile markets among the industrial metals.
Isotopes of Molybdenum
7 isotopes of Molybdenum occur naturally, in the proportions below.
| Isotope | Relative atomic mass | Natural abundance |
|---|---|---|
| 92Mo | 91.90680796(84) | 14.53% |
| 94Mo | 93.9050849(48) | 9.15% |
| 95Mo | 94.90583877(47) | 15.84% |
| 96Mo | 95.90467612(47) | 16.67% |
| 97Mo | 96.90601812(49) | 9.6% |
| 98Mo | 97.90540482(49) | 24.39% |
| 100Mo | 99.9074718(11) | 9.82% |
42
Mo
Molybdenum
transition metal
- Standard atomic weight
- 95.95(1)
- Group / period / block
- 6 · 5 · d
- Electron configuration
- [Kr] 5s1 4d5
- Electrons per shell
- 2, 8, 18, 13, 1
- State at 20 °C
- solid
- Melting point
- 2896 K · 2623 °C
- Boiling point
- 4912 K · 4639 °C
- Density
- 10.2 g/cm³
- Electronegativity
- 2.16 (Pauling)
- First ionisation energy
- 7.092 eV
- Common oxidation states
- +6
- Discovery
- 1778 · credited to Carl Wilhelm Scheele
Hazard facts
No flag in this site’s hazard vocabulary applies to Molybdenum. That is not the same as harmless: it means none of the eleven categories used here — reactive with water, pyrophoric, flammable, oxidising, corrosive, irritant, acutely toxic, accumulating in the body, carcinogenic, asphyxiant or radioactive — is on record for the element itself.
These are properties of the element, stated as facts. Nothing on this site describes how to handle or work with any substance.