Barium

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

Not to be confused with Baryon.
Barium, 56Ba
Barium
Pronunciation/ˈbɛəriəm/ ​(BAIR-ee-əm)
Appearancesilvery gray; with a pale yellow tint[1]
Standard atomic weight Ar°(Ba)
  • 137.327±0.007
  • 137.33±0.01 (abridged)[2]
Barium in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
 Sr
↑
Ba
↓
Ra
caesium ← barium → lanthanum
Atomic number (Z)56
Groupgroup 2 (alkaline earth metals)
Periodperiod 6
Block  s-block
Electron configuration[Xe] 6s2
Electrons per shell2, 8, 18, 18, 8, 2
Physical properties
Phase at STPsolid
Melting point1000 K ​(727 °C, ​1341 °F)
Boiling point2118 K ​(1845 °C, ​3353 °F)
Density (near r.t.)3.51 g/cm3
when liquid (at m.p.)3.338 g/cm3
Heat of fusion7.12 kJ/mol
Heat of vaporization142 kJ/mol
Molar heat capacity28.07 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 911 1038 1185 1388 1686 2170
Atomic properties
Oxidation states+1, +2 (a strongly basic oxide)
ElectronegativityPauling scale: 0.89
Ionization energies
  • 1st: 502.9 kJ/mol
  • 2nd: 965.2 kJ/mol
  • 3rd: 3600 kJ/mol
Atomic radiusempirical: 222 pm
Covalent radius215±11 pm
Van der Waals radius268 pm
Spectral lines of barium
Other properties
Natural occurrenceprimordial
Crystal structure ​body-centered cubic (bcc)
Speed of sound thin rod1620 m/s (at 20 °C)
Thermal expansion20.6 µm/(m⋅K) (at 25 °C)
Thermal conductivity18.4 W/(m⋅K)
Electrical resistivity332 nΩ⋅m (at 20 °C)
Magnetic orderingparamagnetic[3]
Molar magnetic susceptibility+20.6×10−6 cm3/mol[4]
Young's modulus13 GPa
Shear modulus4.9 GPa
Bulk modulus9.6 GPa
Mohs hardness1.25
CAS Number7440-39-3
History
DiscoveryCarl Wilhelm Scheele (1772)
First isolationHumphry Davy (1808)
Main isotopes of barium
Iso­tope Abun­dance Half-life (t1/2) Decay mode Pro­duct
130Ba 0.11% (0.5–2.7)×1021 y εε 130Xe
132Ba 0.10% stable
133Ba syn 10.51 y ε 133Cs
134Ba 2.42% stable
135Ba 6.59% stable
136Ba 7.85% stable
137Ba 11.23% stable
138Ba 71.70% stable

The most common minerals of barium are baryte (barium sulfate, BaSO4) and witherite (barium carbonate, BaCO3). The name barium originates from the alchemical derivative "baryta", from Greek βαρὺς (barys), meaning 'heavy'. Baric is the adjectival form of barium. Barium was identified as a new element in 1774, but not reduced to a metal until 1808 with the advent of electrolysis.

Barium has few industrial applications. Historically, it was used as a getter for vacuum tubes and in oxide form as the emissive coating on indirectly heated cathodes. It is a component of YBCO (high-temperature superconductors) and electroceramics, and is added to steel and cast iron to reduce the size of carbon grains within the microstructure. Barium compounds are added to fireworks to impart a green color. Barium sulfate is used as an insoluble additive to oil well drilling fluid. In a purer form it is used as X-ray radiocontrast agents for imaging the human gastrointestinal tract. Water-soluble barium compounds are poisonous and have been used as rodenticides.

Characteristics

Physical properties
Oxidized barium

Barium is a soft, silvery-white metal, with a slight golden shade when ultrapure.[5]: 2  The silvery-white color of barium metal rapidly vanishes upon oxidation in air yielding a dark gray layer containing the oxide. Barium has a medium specific weight and high electrical conductivity. Because barium is difficult to purify, many of its properties have not been accurately determined.[5]: 2 

At room temperature and pressure, barium metal adopts a body-centered cubic structure, with a barium–barium distance of 503 picometers, expanding with heating at a rate of approximately 1.8×10−5/°C.[5]: 2  It is a very soft metal with a Mohs hardness of 1.25.[5]: 2  Its melting temperature of 1,000 K (730 °C; 1,340 °F)[6]: 4–43  is intermediate between those of the lighter strontium (1,050 K or 780 °C or 1,430 °F)[6]: 4–86  and heavier radium (973 K or 700 °C or 1,292 °F);[6]: 4–78  however, its boiling point of 2,170 K (1,900 °C; 3,450 °F) exceeds that of strontium (1,655 K or 1,382 °C or 2,519 °F).[6]: 4–86  The density (3.62 g/cm3)[6]: 4–43  is again intermediate between those of strontium (2.36 g/cm3)[6]: 4–86  and radium (≈5 g/cm3).[6]: 4–78 

Chemical reactivity

Barium is chemically similar to magnesium, calcium, and strontium, but even more reactive. It is usually found in the +2 oxidation state. Most exceptions are in a few rare and unstable molecular species that are only characterised in the gas phase such as BaF,[5]: 2  but recently a barium(I) species has been reported in a graphite intercalation compound.[7] Reactions with chalcogens are highly exothermic (release energy); the reaction with oxygen or air occurs at room temperature. For this reason, metallic barium is often stored under oil or in an inert atmosphere.[5]: 2  Reactions with other nonmetals, such as carbon, nitrogen, phosphorus, silicon, and hydrogen, are generally exothermic and proceed upon heating.[5]: 2–3  Reactions with water and alcohols are very exothermic and release hydrogen gas:[5]: 3 

Ba + 2 ROH → Ba(OR)2 + H2↑ (R is an alkyl group or a hydrogen atom)

Barium reacts with ammonia to form complexes such as Ba(NH3)6.[5]: 3 

The metal is readily attacked by acids. Sulfuric acid is a notable exception because passivation stops the reaction by forming the insoluble barium sulfate on the surface.[8] Barium combines with several other metals, including aluminium, zinc, lead, and tin, forming intermetallic phases and alloys.[9]

Compounds
Selected alkaline earth and zinc salts densities, g/cm3
O2−
 S2−
 F−
 Cl−
 SO2−
4		 CO2−
3		 O2−
2		 H−
Ca2+
[6]: 4–48–50 		 3.34 2.59 3.18 2.15 2.96 2.83 2.9 1.7
Sr2+
[6]: 4–86–88 		 5.1 3.7 4.24 3.05 3.96 3.5 4.78 3.26
Ba2+
[6]: 4–43–45 		 5.72 4.3 4.89 3.89 4.49 4.29 4.96 4.16
Zn2+
[6]: 4–95–96 		 5.6 4.09 4.95 2.09 3.54 4.4 1.57 —

Barium salts are typically white when solid and colorless when dissolved.[10] They are denser than the strontium or calcium analogs, except for the halides (see table; zinc is given for comparison).

Barium hydroxide ("baryta") was known to alchemists, who produced it by heating barium carbonate. Unlike calcium hydroxide, it absorbs very little CO2 in aqueous solutions and is therefore insensitive to atmospheric fluctuations. This property is used in calibrating pH equipment.

Volatile barium compounds burn with a green to pale green flame, which is an efficient test to detect a barium compound. The color results from spectral lines at 455.4, 493.4, 553.6, and 611.1 nm.[5]: 3 

Organobarium compounds are a growing field of knowledge: recently discovered are dialkylbariums and alkylhalobariums.[5]: 3 

Isotopes

Barium found in the Earth's crust is a mixture of seven primordial nuclides, barium-130, 132, and 134 through 138.[11] Barium-130 undergoes very slow radioactive decay to xenon-130 by double beta plus decay, with a half-life of (0.5–2.7)×1021 years (about 1011 times the age of the universe). Its abundance is ≈0.1% that of natural barium.[11] Theoretically, barium-132 can similarly undergo double beta decay to xenon-132; this decay has not been detected.[12] The radioactivity of these isotopes are so weak that they pose no danger to life.

Of the stable isotopes, barium-138 composes 71.7% of all barium; other isotopes have decreasing abundance with decreasing mass number.[11]

In total, barium has 40 known isotopes, ranging in mass between 114 and 153. The most stable artificial radioisotope is barium-133 with a half-life of approximately 10.51 years. Five other isotopes have half-lives longer than a day.[12] Barium also has 10 meta states, of which barium-133m1 is the most stable with a half-life of about 39 hours.[12]

History
Sir Humphry Davy, who first isolated barium metal

Alchemists in the early Middle Ages knew about some barium minerals. Smooth pebble-like stones of mineral baryte were found in volcanic rock near Bologna, Italy, and so were called "Bologna stones". Alchemists were attracted to them because after exposure to light they would glow for years.[13] The phosphorescent properties of baryte heated with organics were described by V. Casciorolus in 1602.[5]: 5 

Carl Scheele determined that baryte contained a new element in 1774, but could not isolate barium, only barium oxide. Johan Gottlieb Gahn also isolated barium oxide two years later in similar studies. Oxidized barium was at first called "barote" by Guyton de Morveau, a name that was changed by Antoine Lavoisier to baryta. Also in the 18th century, English mineralogist William Withering noted a heavy mineral in the lead mines of Cumberland, now known to be witherite. Barium was first isolated by electrolysis of molten barium salts in 1808 by Sir Humphry Davy in England.[14] Davy, by analogy with calcium, named "barium" after baryta, with the "-ium" ending signifying a metallic element.[13] Robert Bunsen and Augustus Matthiessen obtained pure barium by electrolysis of a molten mixture of barium chloride and ammonium chloride.[15][16]

The production of pure oxygen in the Brin process was a large-scale application of barium peroxide in the 1880s, before it was replaced by electrolysis and fractional distillation of liquefied air in the early 1900s. In this process barium oxide reacts at 500–600 °C (932–1,112 °F) with air to form barium peroxide, which decomposes above 700 °C (1,292 °F) by releasing oxygen:[17][18]

2 BaO + O2 ⇌ 2 BaO2

Barium sulfate was first applied as a radiocontrast agent in X-ray imaging of the digestive system in 1908.[19]

Occurrence and production

The abundance of barium is 0.0425% in the Earth's crust and 13 μg/L in sea water. The primary commercial source of barium is baryte (also called barytes or heavy spar), a barium sulfate mineral.[5]: 5  with deposits in many parts of the world. Another commercial source, far less important than baryte, is witherite, barium carbonate. The main deposits are located in Britain, Romania, and the former USSR.[5]: 5 

Barite, left to right: appearance, graph showing trends in production over time, and the map showing shares of the most important producer countries in 2010.

The baryte reserves are estimated between 0.7 and 2 billion tonnes. The maximum production, 8.3 million tonnes, was produced in 1981, but only 7–8% was used for barium metal or compounds.[5]: 5  Baryte production has risen since the second half of the 1990s from 5.6 million tonnes in 1996 to 7.6 in 2005 and 7.8 in 2011. China accounts for more than 50% of this output, followed by India (14% in 2011), Morocco (8.3%), US (8.2%), Turkey (2.5%), Iran and Kazakhstan (2.6% each).[20]

The mined ore is washed, crushed, classified, and separated from quartz. If the quartz penetrates too deeply into the ore, or the iron, zinc, or lead content is abnormally high, then froth flotation is used. The product is a 98% pure baryte (by mass); the purity should be no less than 95%, with a minimal content of iron and silicon dioxide.[5]: 7  It is then reduced by carbon to barium sulfide:[5]: 6 

BaSO4 + 2 C → BaS + 2 CO2

The water-soluble barium sulfide is the starting point for other compounds: treating BaS with oxygen produces the sulfate, with nitric acid the nitrate, with aqueous carbon dioxide the carbonate, and so on.[5]: 6  The nitrate can be thermally decomposed to yield the oxide.[5]: 6  Barium metal is produced by reduction with aluminium at 1,100 °C (2,010 °F). The intermetallic compound BaAl4 is produced first:[5]: 3 

3 BaO + 14 Al → 3 BaAl4 + Al2O3

BaAl4 is an intermediate reacted with barium oxide to produce the metal. Note that not all barium is reduced.[5]: 3 

8 BaO + BaAl4 → Ba↓ + 7 BaAl2O4

The remaining barium oxide reacts with the formed aluminium oxide:[5]: 3 

BaO + Al2O3 → BaAl2O4

and the overall reaction is[5]: 3 

4 BaO + 2 Al → 3 Ba↓ + BaAl2O4

Barium vapor is condensed and packed into molds in an atmosphere of argon.[5]: 3  This method is used commercially, yielding ultrapure barium.[5]: 3  Commonly sold barium is about 99% pure, with main impurities being strontium and calcium (up to 0.8% and 0.25%) and other contaminants contributing less than 0.1%.[5]: 4 

A similar reaction with silicon at 1,200 °C (2,190 °F) yields barium and barium metasilicate.[5]: 3  Electrolysis is not used because barium readily dissolves in molten halides and the product is rather impure.[5]: 3 

Benitoite crystals on natrolite. The mineral is named for the San Benito River in San Benito County where it was first found.

Gemstone

The barium mineral, benitoite (barium titanium silicate), occurs as a very rare blue fluorescent gemstone, and is the official state gem of California.

Barium in seawater

Barium exists in seawater as the Ba2+ ion with an average oceanic concentration of 109 nmol/kg.[21] Barium also exists in the ocean as BaSO4, or barite.[22] Barium has a nutrient-like profile[23] with a residence time of 10,000 years.[21]

Barium shows a relatively consistent concentration in upper ocean seawater, excepting regions of high river inputs and regions with strong upwelling.[24] There’s little depletion of barium concentrations in the upper ocean for an ion with a nutrient-like profile, thus lateral mixing is important.[24] Barium isotopic values show basin-scale balances instead of local or short-term processes.[24]

Applications

Metal and alloys

Barium, as a metal or when alloyed with aluminium, is used to remove unwanted gases (gettering) from vacuum tubes, such as TV picture tubes.[5]: 4  Barium is suitable for this purpose because of its low vapor pressure and reactivity towards oxygen, nitrogen, carbon dioxide, and water; it can even partly remove noble gases by dissolving them in the crystal lattice. This application is gradually disappearing due to the rising popularity of the tubeless LCD and plasma sets.[5]: 4 

Other uses of elemental barium are minor and include an additive to silumin (aluminium–silicon alloys) that refines their structure, as well as[5]: 4 

  • bearing alloys;
  • lead–tin soldering alloys – to increase the creep resistance;
  • alloy with nickel for spark plugs;
  • additive to steel and cast iron as an inoculant;
  • alloys with calcium, manganese, silicon, and aluminium as high-grade steel deoxidizers.

Barium sulfate and baryte
Amoebiasis as seen in a radiograph of a barium-filled colon

Barium sulfate (the mineral baryte, BaSO4) is important to the petroleum industry as a drilling fluid in oil and gas wells.[6]: 4–5  The precipitate of the compound (called "blanc fixe", from the French for "permanent white") is used in paints and varnishes; as a filler in ringing ink, plastics, and rubbers; as a paper coating pigment; and in nanoparticles, to improve physical properties of some polymers, such as epoxies.[5]: 9 

Barium sulfate has a low toxicity and relatively high density of ca. 4.5 g/cm3 (and thus opacity to X-rays). For this reason it is used as a radiocontrast agent in X-ray imaging of the digestive system ("barium meals" and "barium enemas").[6]: 4–5  Lithopone, a pigment that contains barium sulfate and zinc sulfide, is a permanent white with good covering power that does not darken when exposed to sulfides.[25]

Other barium compounds
Green barium fireworks

Other compounds of barium find only niche applications, limited by the toxicity of Ba2+ ions (barium carbonate is a rat poison), which is not a problem for the insoluble BaSO4.

  • Barium oxide coating on the electrodes of fluorescent lamps facilitates the release of electrons.
  • By its great atomic density, barium carbonate increases the refractive index and luster of glass[6]: 4–5  and reduces leaks of X-rays from cathode ray tubes (CRT) TV sets.[5]: 12–13 
  • Barium, typically as barium nitrate imparts a yellow or "apple" green color to fireworks;[26] for brilliant green barium monochloride is used.
  • Barium peroxide is a catalyst in the aluminothermic reaction (thermite) for welding rail tracks. It is also a green flare in tracer ammunition and a bleaching agent.[27]
  • Barium titanate is a promising electroceramic.[28]
  • Barium fluoride is used for optics in infrared applications because of its wide transparency range of 0.15–12 micrometers.[29]
  • YBCO was the first high-temperature superconductor cooled by liquid nitrogen, with a transition temperature of 93 K (−180.2 °C; −292.3 °F) that exceeded the boiling point of nitrogen (77 K or −196.2 °C or −321.1 °F).[30]
  • Ferrite, a type of sintered ceramic composed of iron oxide (Fe2O3) and barium oxide (BaO), is both electrically nonconductive and ferrimagnetic, and can be temporarily or permanently magnetized.

Palaeoceanography

The lateral mixing of barium is caused by water mass mixing and ocean circulation.[31] Global ocean circulation reveals a strong correlation between dissolved barium and silicic acid.[31] The large-scale ocean circulation combined with remineralization of barium show a similar correlation between dissolved barium and ocean alkalinity.[31]

Dissolved barium's correlation with silicic acid can be seen both vertically and spatially.[32] Particulate barium shows a strong correlation with particulate organic carbon or POC.[32] Barium is becoming more popular to be used a base for palaeoceanographic proxies.[32] With both dissolved and particulate barium's links with silicic acid and POC, it can be used to determine historical variations in the biological pump, carbon cycle, and global climate.[32]

The barium particulate barite (BaSO4), as one of many proxies, can be used to provide a host of historical information on processes in different oceanic settings (water column, sediments, and hydrothermal sites).[22] In each setting there are differences in isotopic and elemental composition of the barite particulate.[22] Barite in the water column, known as marine or pelagic barite, reveals information on seawater chemistry variation over time.[22] Barite in sediments, known as diagenetic or cold seeps barite, gives information about sedimentary redox processes.[22] Barite formed via hydrothermal activity at hydrothermal vents, known as hydrothermal barite, reveals alterations in the condition of the earth's crust around those vents.[22]

Toxicity
Barium
Hazards
GHS labelling:[33]
Danger
Hazard statements
 H228, H260, H301, H314
Precautionary statements
 P210, P231+P232, P260, P280, P303+P361+P353, P304+P340+P310, P305+P351+P338
NFPA 704 (fire diamond)
0
3
1

Because of the high reactivity of the metal, toxicological data are available only for compounds.[34] Soluble barium compounds are poisonous. In low doses, barium ions act as a muscle stimulant, and higher doses affect the nervous system, causing cardiac irregularities, tremors, weakness, anxiety, shortness of breath, and paralysis. This toxicity may be caused by Ba2+ blocking potassium ion channels, which are critical to the proper function of the nervous system.[35] Other organs damaged by water-soluble barium compounds (i.e., barium ions) are the eyes, immune system, heart, respiratory system, and skin[34] causing, for example, blindness and sensitization.[34]

Barium is not carcinogenic[34] and does not bioaccumulate.[36][37] Inhaled dust containing insoluble barium compounds can accumulate in the lungs, causing a benign condition called baritosis.[38] The insoluble sulfate is nontoxic and is not classified as a dangerous goods in transport regulations.[5]: 9 

To avoid a potentially vigorous chemical reaction, barium metal is kept in an argon atmosphere or under mineral oils. Contact with air is dangerous and may cause ignition. Moisture, friction, heat, sparks, flames, shocks, static electricity, and exposure to oxidizers and acids should be avoided. Anything that may contact with barium should be electrically grounded. Anyone who works with the metal should wear pre-cleaned non-sparking shoes, flame-resistant rubber clothes, rubber gloves, apron, goggles, and a gas mask. Smoking in the working area is typically forbidden. Thorough washing is required after handling barium.[34]

See also
  • Han purple and Han blue – synthetic barium copper silicate pigments developed and used in ancient and imperial China

References
  1. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 112. ISBN 978-0-08-037941-8.
  2. "Standard Atomic Weights: Barium". CIAAW. 1985.
  3. Lide, D. R., ed. (2005). "Magnetic susceptibility of the elements and inorganic compounds". CRC Handbook of Chemistry and Physics (PDF) (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  4. Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN 0-8493-0464-4.
  5. Kresse, Robert; Baudis, Ulrich; Jäger, Paul; Riechers, H. Hermann; Wagner, Heinz; Winkler, Jochen; Wolf, Hans Uwe. "Barium and Barium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_325.pub2.
  6. Lide, D. R. (2004). CRC Handbook of Chemistry and Physics (84th ed.). Boca Raton (FL): CRC Press. ISBN 978-0-8493-0484-2.
  7. W. Xu and M. Lerner, "A New and Facile Route Using Electride Solutions To Intercalate Alkaline Earth Ions into Graphite" Chemistry of Materials 2018 30 (19), 6930-6935 https://DOI.org/10.1021/acs.chemmater.8b03421
  8. Müller, Hermann. "Sulfuric Acid and Sulfur Trioxide". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a25_635.
  9. Ferro, Riccardo & Saccone, Adriana (2008). Intermetallic Chemistry. Elsevier. p. 355. ISBN 978-0-08-044099-6.
  10. Slowinski, Emil J.; Masterton, William L. (1990). Qualitative analysis and the properties of ions in aqueous solution (2nd ed.). Saunders. p. 87. ISBN 978-0-03-031234-2.
  11. de Laeter, John Robert; Böhlke, John Karl; De Bièvre, Paul; Hidaka, Hiroshi; Peiser, H. Steffen; Rosman, Kevin J. R.; Taylor, Philip D. P. (2003). "Atomic weights of the elements. Review 2000 (IUPAC Technical Report)". Pure and Applied Chemistry. 75 (6): 683–800. doi:10.1351/pac200375060683.
  12. Audi, G.; Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S. (2017). "The NUBASE2016 evaluation of nuclear properties" (PDF). Chinese Physics C. 41 (3): 030001. Bibcode:2017ChPhC..41c0001A. doi:10.1088/1674-1137/41/3/030001.
  13. Krebs, Robert E. (2006). The history and use of our earth's chemical elements: a reference guide. Greenwood Publishing Group. p. 80. ISBN 978-0-313-33438-2.
  14. Davy, H (1808). "Electro-chemical researches on the decomposition of the earths; with observations on the metals obtained from the alkaline earths, and on the amalgam procured from ammonia". Philosophical Transactions of the Royal Society of London. 98: 333–370. Bibcode:1808RSPT...98..333D. doi:10.1098/rstl.1808.0023.
  15. "Masthead". Annalen der Chemie und Pharmacie. 93 (3): fmi. 1855. doi:10.1002/jlac.18550930301.
  16. Wagner, Rud; Neubauer, C.; Deville, H. Sainte-Claire; Sorel; Wagenmann, L.; Techniker; Girard, Aimé (1856). "Notizen". Journal für Praktische Chemie. 67: 490–508. doi:10.1002/prac.18560670194.
  17. Jensen, William B. (2009). "The Origin of the Brin Process for the Manufacture of Oxygen". Journal of Chemical Education. 86 (11): 1266. Bibcode:2009JChEd..86.1266J. doi:10.1021/ed086p1266.
  18. Ihde, Aaron John (1984-04-01). The development of modern chemistry. p. 681. ISBN 978-0-486-64235-2.
  19. Schott, G. D. (1974). "Some Observations on the History of the Use of Barium Salts in Medicine". Med. Hist. 18 (1): 9–21. doi:10.1017/S0025727300019190. PMC 1081520. PMID 4618587.
  20. Miller, M. M. Barite. USGS.gov
  21. "Barium". www.mbari.org. Retrieved 2020-11-24.
  22. Griffith, Elizabeth M.; Paytan, Adina (2012). "Barite in the ocean – occurrence, geochemistry and palaeoceanographic applications". Sedimentology. 59 (6): 1817–1835. Bibcode:2012Sedim..59.1817G. doi:10.1111/j.1365-3091.2012.01327.x. ISSN 1365-3091. S2CID 28056031.
  23. "Graph". www.mbari.org. Retrieved 2020-11-24.
  24. Hsieh, Yu-Te; Henderson, Gideon M. (2017). "Barium stable isotopes in the global ocean: Tracer of Ba inputs and utilization". Earth and Planetary Science Letters. 473: 269–278. Bibcode:2017E&PSL.473..269H. doi:10.1016/j.epsl.2017.06.024.
  25. Jones, Chris J. & Thornback, John (2007). Medicinal applications of coordination chemistry. Royal Society of Chemistry. p. 102. ISBN 978-0-85404-596-9.
  26. Russell, Michael S. & Svrcula, Kurt (2008). Chemistry of Fireworks. Royal Society of Chemistry. p. 110. ISBN 978-0-85404-127-5.
  27. Brent, G. F.; Harding, M. D. (1995). "Surfactant coatings for the stabilization of barium peroxide and lead dioxide in pyrotechnic compositions". Propellants, Explosives, Pyrotechnics. 20 (6): 300. doi:10.1002/prep.19950200604.
  28. Wadhawan, Vinod K. (2000). Introduction to ferroic materials. CRC Press. p. 740. ISBN 978-90-5699-286-6.
  29. "Crystran Ltd. Optical Component Materials". crystran.co.uk. Retrieved 2010-12-29.
  30. Wu, M.; Ashburn, J.; Torng, C.; Hor, P.; Meng, R.; Gao, L.; Huang, Z.; Wang, Y.; Chu, C. (1987). "Superconductivity at 93 K in a New Mixed-Phase Y-Ba-Cu-O Compound System at Ambient Pressure". Physical Review Letters. 58 (9): 908–910. Bibcode:1987PhRvL..58..908W. doi:10.1103/PhysRevLett.58.908. PMID 10035069.
  31. Pyle, Kimberley M.; Hendry, Katharine R.; Sherrell, Robert M.; Legge, Oliver; Hind, Andrew J.; Bakker, Dorothee; Venables, Hugh; Meredith, Michael P. (2018-08-20). "Oceanic fronts control the distribution of dissolved barium in the Southern Ocean". Marine Chemistry. 204: 95–106. doi:10.1016/j.marchem.2018.07.002. ISSN 0304-4203. S2CID 104170533.
  32. Bates, Stephanie L.; Hendry, Katharine R.; Pryer, Helena V.; Kinsley, Christopher W.; Pyle, Kimberley M.; Woodward, E. Malcolm S.; Horner, Tristan J. (2017-05-01). "Barium isotopes reveal role of ocean circulation on barium cycling in the Atlantic". Geochimica et Cosmochimica Acta. 204: 286–299. Bibcode:2017GeCoA.204..286B. doi:10.1016/j.gca.2017.01.043. hdl:1912/8676. ISSN 0016-7037. S2CID 55559902.
  33. "Barium 237094". Sigma-Aldrich. 2021-10-28. Retrieved 2021-12-21.
  34. Barium. ESPI Metals. Retrieved 2012-06-11.
  35. Patnaik, Pradyot (2003). Handbook of inorganic chemicals. McGraw-Hill. pp. 77–78. ISBN 978-0-07-049439-8.
  36. "Toxicity Profiles, Ecological Risk Assessment". US EPA. Archived from the original on 2010-01-10. Retrieved 2012-06-16.
  37. Moore, J. W. (1991). Inorganic Contaminants of Surface Waters, Research and Monitoring Priorities. New York: Springer-Verlag.
  38. Doig, A. T. (1976). "Baritosis: a benign pneumoconiosis". Thorax. 31 (1): 30–9. doi:10.1136/thx.31.1.30. PMC 470358. PMID 1257935.

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