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560.890
137.328 u+2
[Xe] 6s2BaBarium

Barium

Barium is a chemical element with symbol Ba and atomic number 56. It is the fifth element in Group 2, a soft silvery metallic alkaline earth metal. Because of its high chemical reactivity barium is never found in nature as a free element.

Identity

Atomic mass
137.328 u
Category
Alkaline earth metals
Group
2
Period
6
Block
s
Oxidation States
+2
Phase (25 °C)
Solid

Electronic Structure

Electron configuration
1s2 2s2 2p6 3s2 3p6 4s2 3d10 4p6 5s2 4d10 5p6 6s2
Short configuration
[Xe] 6s2
Electrons per shell
2, 8, 18, 18, 8, 2
Electronegativity (Pauling)
0.890
Electron affinity
14.0 kJ/mol
1st ionization energy
503 kJ/mol
Ionization energies
503 · 965 · 3600 kJ/mol

Physical properties

Melting point
726.9 °C (1000 K)
Boiling point
1844.8 °C (2118 K)
Density
3.51 g/cm³
Molar heat capacity
28.1 J/(mol·K)

Chemical behavior of barium

Barium has two valence electrons in the 6s orbital ([Xe] 6s²). Its ionization energy is very low and it quickly gives up both electrons to form the divalent Ba²⁺ cation with a noble gas configuration (xenon). It belongs to group 2 of the alkaline earth metals, located below strontium. It is the least reactive and most electropositive alkaline earth metal in the periodic table. It forms markedly ionic bonds. In presence of oxygen or atmospheric moisture it oxidises quickly, acquiring a matte grey coating, and burns easily emitting a characteristic green apple flame.

Reactivity

  • Ba + 2 H₂O → Ba(OH)₂ + H₂

    It reacts rapidly and very exothermically with liquid water, releasing hydrogen gas and forming soluble barium hydroxide.

  • 2 Ba + O₂ → 2 BaO

    When heated, it burns vigorously in air with a striking yellowish-green luminous emission, producing barium oxide and barium peroxide.

  • Ba²⁺ + SO₄²⁻ → BaSO₄

    It reacts almost instantaneously and quantitatively with sulfate anions in water, precipitating barium sulfate, a white solid with the lowest solubility product among alkaline earth metals.

  • Ba + Cl₂ → BaCl₂

    It combines directly with hot chlorine gas to form barium chloride in a strongly exothermic reaction.

Notable compounds

CompoundFormulaUse or importance
Barium sulfateBaSO₄Barite; opaque X-ray contrast medium for the digestive tract, drilling muds and white pigment (lithopone)
Barium titanateBaTiO₃Fundamental ceramic ferroelectric and piezoelectric material in multilayer ceramic capacitors and ultrasound transducers
Barium nitrateBa(NO₃)₂Oxidizing salt used in pyrotechnics to generate brilliant green color in fireworks and tracer projectiles
Barium hydroxideBa(OH)₂Caustic baryta; soluble alkaline analytical reagent for titrating acids and precipitating insoluble carbonates

Electron shell distribution

Electron shell distribution diagram of Barium.Bohr-style diagram: the nucleus sits at the center and the electrons are arranged on concentric circular orbits, one per energy level.BaView in the atom builder

Isotopes

Natural barium is composed of seven isotopes: six stable (¹³⁰Ba, ¹³²Ba, ¹³⁴Ba, ¹³⁵Ba, ¹³⁶Ba, ¹³⁷Ba and ¹³⁸Ba, with ¹³⁸Ba being the most abundant at 71.70% and a magic number of 82 neutrons) and a primordial radionuclide with extremely long half-life (¹³⁰Ba). About forty radioisotopes have been synthesised; among them, barium-133 (¹³³Ba, half-life of 10.5 years) is used as a standardised gamma source for calibrating nuclear physics equipment and medical detectors.

Occurrence and production

It is the 14th most abundant element in the Earth's crust (about 425-450 ppm). It does not exist free due to its high chemical reactivity. Its main mineral ore is barite or heavy spar (barium sulfate, BaSO₄), characterised by its extraordinary density for a non-metallic mineral; another secondary source is witherite (barium carbonate, BaCO₃). The world's largest producers are China, India and Morocco. The metal is obtained by thermal reduction of barium oxide with metallic aluminium at 1100 °C in vacuum furnaces.

History and origin of the name

In 1602, the Bologna cobbler and alchemist Vincenzo Cascariolo heated barite stones with coal, obtaining a material that glowed in the dark ('Bologna stone'), discovering the first synthetic phosphorescent material. In 1774, Carl Wilhelm Scheele identified barium oxide as a new mineral earth in pyrolusite, and in 1808 Humphry Davy first isolated metallic barium by electrolysis of molten barium hydroxide. Davy named 'barium' from the Greek 'barys' (heavy), in reference to the remarkable density of its minerals.

Applications and relevance of barium

Uses of the element

Pure metallic barium is mainly used as a degasser or 'getter' in vacuum tubes, cathode-ray tubes and radio-frequency thermionic valves, where its extremely high reactivity chemically absorbs microscopic traces of residual gases (oxygen, nitrogen, water vapour). It is also incorporated in small doses in lead and tin alloys for anti-friction bearings and in spark plugs for high-speed internal combustion engines.

Uses of its compounds

More than 80% of the world's barium sulfate is consumed as a density agent in drilling muds for deep oil and gas drilling. In medicine it is the quintessential X-ray contrast medium for stomach and intestine radiographs; barium titanate is used in millions of multilayer ceramic capacitors for telecommunications; and nitrate salts colour fireworks green.

Health, safety and environment

Biological role

It is not an essential element for human or animal life. Soluble barium ions (Ba²⁺) are extremely toxic because they competitively block potassium channels in cell membranes, causing muscle paralysis, serious cardiac arrhythmias and acute arterial hypertension.

Safety

Despite the toxicity of free cations, barium sulfate ingested in medical radiological examinations is absolutely safe and harmless thanks to its extreme chemical insolubility (solubility product constant of 10⁻¹⁰), preventing ion absorption into the blood. In contrast, soluble salts such as barium chloride or carbonate can be fatal if accidentally ingested.

Environment

Natural barite is mineralogically inert and does not represent ecological risk. Industrial wastewaters containing soluble barium must be treated by precipitation with sulphates to immobilise the cation as insoluble barite before any discharge.

Frequently asked questions about Barium

Why is it said to drink a barium liquid before a digestive radiography?

Although dissolved barium is toxic, the medical 'barium meal' taken before a digestive test contains barium sulfate, a practically water and gastric juice insoluble compound. It passes through the stomach and intestines without being absorbed by the body. Because barium is a heavy atom that blocks X-rays, it draws with enormous contrast the relief of the organs in the images.

How do heavy barite muds prevent blowouts in oil wells?

During drilling of natural gas or crude oil wells at thousands of metres deep, ground barite (with a density of 4.5 g/cm³) is added to the drilling fluid. This dense mixture exerts a colossal hydrostatic pressure at the well bottom that exceeds the geological pressure of underground gas and oil pockets. This fluid weight confines the hydrocarbons in the reservoir, preventing uncontrolled gas eruptions to the surface that would cause explosions.

Why did barium titanate revolutionise modern electronic capacitors?

Barium titanate (BaTiO₃) is a ceramic that exhibits ferroelectricity with an enormously large dielectric constant at room temperature, exceeding by thousands of times that of traditional insulators such as mica or glass. When an electric field is applied, titanium and barium ions move within the crystal cell generating a reversible spontaneous polarisation. This property allows the manufacture of microscopic multilayer ceramic capacitors (MLCCs) capable of storing great electrical charge in smartphones and computers.

What do barium 'getters' consist of that preserved the vacuum in old televisions?

In old cathode-ray tubes for televisions and radio valves, it was essential to maintain an almost perfect vacuum for electrons to travel without colliding with gas molecules. At the end of the tube's manufacture, a small barium pellet volatilised by radio frequency induction, depositing a bright metallic mirror on the inner glass. This highly reactive barium film chemically captured any residual oxygen, nitrogen or water molecule for years.

What was the legendary 'Bologna stone' and what role did it play in the discovery of phosphorescence?

In the early 17th century in Italy, the amateur alchemist Vincenzo Cascariolo collected dense nodules of barite on Mount Paderno and calcined them with coal in his forge. The process reduced the barium sulfate to impure barium sulfide, creating an insoluble material that, after exposure to daylight, shone intensely in the dark for hours. That 'Bologna phosphorescent stone' fascinated European scientists, inaugurating the formal study of inorganic luminescence.

How do soluble barium ions block potassium channels causing neuromuscular toxicity?

The divalent Ba²⁺ cation has an ionic radius very similar to that of potassium (K⁺). When it enters the bloodstream from ingested soluble salts, it fits perfectly into the selectivity filter of voltage-gated potassium channels in muscle and cardiac cells, lodging there and blocking potassium exit. This inhibition prolongs cell depolarisation, triggering severe hypokalaemia, involuntary tetanic muscle contractions, flaccid respiratory paralysis and fatal cardiac arrests.

Why do green fireworks contain barium?

The brilliant green colour of pyrotechnics is due to compounds such as barium nitrate or barium chloride. When the gunpowder detonates and heats the mixture to over a thousand degrees, barium electrons are excited and, when returning to their original state, release excess energy by emitting light at a very pure emerald green wavelength highly visible in the night sky.

Main sources consulted: PubChem, Royal Society of Chemistry, NIST, IUPAC. Last revision: November 2026.