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barium

 
(bâr'ē-əm, băr'-) pronunciation
n. (Symbol Ba)
A soft, silvery-white alkaline-earth metal, used to deoxidize copper and in various alloys. Atomic number 56; atomic weight 137.33; melting point 725°C; boiling point 1,140°C; specific gravity 3.50; valence 2.

[BAR(YTA) + -IUM.]

baric bar'ic (-ĭk) adj.

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Chemical element, one of the alkaline earth metals, chemical symbol Ba, atomic number 56. It is very reactive and in compounds always has valence 2. In nature it is found chiefly as the minerals barite (barium sulfate) and witherite (barium carbonate). The element is used in metallurgy, and its compounds are used in fireworks, petroleum mining, and radiology and as pigments and reagents. All soluble barium compounds are toxic. Barium sulfate, one of the most insoluble salts known, is given in a "barium meal" as a contrast medium for X-ray examination of the gastrointestinal tract.

For more information on barium, visit Britannica.com.

A chemical element, Ba, with atomic number 56 and atomic weight of 137.34. Barium is eighteenth in abundance in the Earth's crust, where it is found to the extent of 0.04%, making it intermediate in amount between calcium and strontium, the other alkaline-earth metals. Barium compounds are obtained from the mining and conversion of two barium minerals. Barite, barium sulfate, is the principal ore and contains 65.79% barium oxide. Witherite, sometimes called heavy spar, is barium carbonate and is 72% barium oxide. See also Periodic table.

The metal was first isolated by Sir Humphry Davy in 1808 by electrolysis. Industrially, only small amounts are prepared by aluminum reduction of barium oxide in large retorts. These are used in barium-nickel alloys for spark-plug wire (the barium increases the emissivity of the alloy) and in frary metal, which is an alloy of lead, barium, and calcium used in place of babbitt metal because it can be cast.

The metal reacts with water more readily than do strontium and calcium, but less readily than sodium; it oxidizes quickly in air to form a surface film that inhibits further reaction, but in moist air it may inflame. The metal is sufficiently active chemically to react with most nonmetals. Freshly cut pieces have a lustrous gray-white appearance, and the metal is both ductile and malleable. The physical properties of the elementary form are given in the table.

Properties of barium

Property

Value

Atomic number

56

Atomic weight

137.34

Isotopes (stable)

130, 132, 134, 135, 136, 137, 138

Atomic volume

36.2 cm3/g-atom

Crystal structure

Face-centered cubic

Electron configuration

2 8 18 18 8 2

Valence

2+

Ionic radius (A)

1.35

Boiling point, °C

1140(?)

Melting point, °C

850(?)

Density

3.75 g/cm3 at 20°C

Latent heat of vaporization at boiling point, kj/g-atom

374

For the manufacture of barium compounds, soft (easily crushable) barite is preferred, but crystalline varieties may be used. Crude barite is crushed and then mixed with pulverized coal. The mixture is roasted in a rotary reduction furnace, and the barium sulfate is thus reduced to barium sulfide or black ash. Black ash is roughly 70% barium sulfide and is treated with hot water to make a solution used as the starting material for the manufacture of many compounds.

Lithopone, a white powder consisting of 20% barium sulfate, 30% zinc sulfide, and less than 3% zinc oxide, is widely used as a pigment in white paints. Blanc fixe is used in the manufacture of brilliant coloring compounds. It is the best grade of barium sulfate for paint pigments. Because of the large absorption of x-rays by barium, the sulfate is used to coat the alimentary tract for x-ray photographs in order to increase the contrast. Barium carbonate is useful in the ceramic industry to prevent efflorescence on claywares. It is used also as a pottery glaze, in optical glass, and in rat poisons. Barium chloride is used in purifying salt brines, in chlorine and sodium hydroxide manufacture, as a flux for magnesium alloys, as a water softener in boiler compounds, and in medicinal preparations. Barium nitrate, or the so-called baryta saltpeter, finds use in pyrotechnics and signal flares (to produce a green color), and to a small extent in medicinal preparations. Barium oxide, known as baryta or calcined baryta, finds use both as an industrial drying agent and in the case-hardening of steels. Barium peroxide is sometimes used as a bleaching agent. Barium chromate, lemon chrome or chrome yellow, is used in yellow pigments and safety matches. Barium chlorate finds use in the manufacture of pyrotechnics. Barium acetate and cyanide are used industrially as a chemical reagent and in metallurgy, respectively.


A metal of no known metabolic function, and hence not a dietary essential. Barium sulphate is opaque to X-rays and a suspension is used (a barium meal) to allow examination of the shape and movements of the stomach for diagnostic purposes, and as a barium enema for X-ray investigation of the lower intestinal tract.

barium (bâr'ēəm) [Gr.,=heavy], metallic chemical element; symbol Ba; at. no. 56; at. wt. 137.327; m.p. 725°C; b.p. 1,640°C; sp. gr. 3.5 at 20°C; valence +2. Barium is a soft, silver-white, chemically active, poisonous metal with a face-centered cubic crystalline structure. It is an alkaline-earth metal in Group 2 of the periodic table. Its principal ore is barite (barium sulfate); it also occurs in the mineral witherite (barium carbonate). The pure metal is obtained by the electrolysis of fused barium salts or, industrially, by the reduction of barium oxide with aluminum. Barium is often used in barium-nickel alloys for spark-plug electrodes and in vacuum tubes as a drying and oxygen-removing agent. Barium oxidizes in air, and it reacts vigorously with water to form the hydroxide, liberating hydrogen. In moist air it may spontaneously ignite. It burns in air to form the peroxide, which produces hydrogen peroxide when treated with water. Barium reacts with almost all of the nonmetals; all of its water-soluble and acid-soluble compounds are poisonous. Barium carbonate is used in glass, as a pottery glaze, and as a rat poison. Chrome yellow (barium chromate) is used as a paint pigment and in safety matches. The chlorate and nitrate are used in pyrotechnics to provide a green color. Barium oxide strongly absorbs carbon dioxide and water; it is used as a drying agent. Barium chloride is used in medicinal preparations and as a water softener. Barium sulfide phosphoresces after exposure to light; it is sometimes used as a paint pigment. Barite, the sulfate ore, has many industrial uses. Because barium sulfate is virtually insoluble in water and acids, it can be used to coat the alimentary tract to increase the contrast for X-ray photography without being absorbed by the body and poisoning the subject. Barium salts give a characteristic green color in the flame test. Barium metal was first isolated in 1808 by Sir Humphry Davy by electrolysis.


A chemical element, atomic number 56, atomic weight 137.34, symbol Ba. Soluble salts, e.g. the chloride and the carbonate, are toxic.

  • b. burger, barium meal — a mixture of barium and solid food, used as a contrast medium in radiographic studies of the esophagus, instead of liquid barium mixtures.
  • b. chloride — used as a rodenticide. The baits are attractive to dogs. Clinical signs include salivation, convulsions and paralysis.
  • b. deficiency — preliminary experiments showing that diets deficient in barium fed to rats and guinea pigs depress growth have been neither invalidated nor confirmed.
  • b. enema — a dilute (5 to 20%) suspension of barium is introduced into a colon that has been emptied by starvation and previous enema.
    Barium enema. By permission from Ettinger SJ, Feldman E, Textbook of Veterinary Internal Medicine, Saunders, 2004
  • b.-impregnated polyethylene spheres (BIPS) — radio-opaque markers used to demonstrate intestinal obstruction and motility disorders; the spheres are given orally and their movement can be tracked radiographically.
  • b. meal — a strong (usually 100%) suspension of barium sulfate is administered to an animal which has been starved for at least 12 hours.
  • b. study — x-ray examination using a barium mixture to help locate disorders in the esophagus, stomach, duodenum, and the small and large intestines. Called also barium test.
  • b. sulfate — a water-insoluble salt used as an opaque contrast medium for x-ray examination of the digestive tract.
  • b. swallow — a small amount of barium paste or liquid administered orally and observed radiographically or by fluoroscopy for examination of swallowing and esophageal function.
  • b. test — barium study.
(ber′ē-əm)
n
Ba

A pale yellow, metallic element classified with the alkaline earths.

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  See crossword solutions for the clue Barium.
caesiumbariumlanthanum
Sr

Ba

Ra
Appearance
silvery gray
General properties
Name, symbol, number barium, Ba, 56
Pronunciation /ˈbɛəriəm/ bair-ee-əm
Element category alkaline earth metals
Group, period, block 26, s
Standard atomic weight 137.33
Electron configuration [Xe] 6s2
Electrons per shell 2, 8, 18, 18, 8, 2 (Image)
Physical properties
Phase solid
Density (near r.t.) 3.51 g·cm−3
Liquid density at m.p. 3.338 g·cm−3
Melting point 1000 K, 727 °C, 1341 °F
Boiling point 2170 K, 1897 °C, 3447 °F
Heat of fusion 7.12 kJ·mol−1
Heat of vaporization 140.3 kJ·mol−1
Molar heat capacity 28.07 J·mol−1·K−1
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 2
(strongly basic oxide)
Electronegativity 0.89 (Pauling scale)
Ionization energies 1st: 502.9 kJ·mol−1
2nd: 965.2 kJ·mol−1
3rd: 3600 kJ·mol−1
Atomic radius 222 pm
Covalent radius 215±11 pm
Van der Waals radius 268 pm
Miscellanea
Crystal structure body-centered cubic
Magnetic ordering paramagnetic
Electrical resistivity (20 °C) 332 nΩ·m
Thermal conductivity 18.4 W·m−1·K−1
Thermal expansion (25 °C) 20.6 µm·m−1·K−1
Speed of sound (thin rod) (20 °C) 1620 m·s−1
Young's modulus 13 GPa
Shear modulus 4.9 GPa
Bulk modulus 9.6 GPa
Mohs hardness 1.25
CAS registry number 7440-39-3
Most stable isotopes
Main article: Isotopes of barium
iso NA half-life DM DE (MeV) DP
130Ba 0.106% 130Ba is stable with 74 neutrons
132Ba 0.101% 132Ba is stable with 76 neutrons
133Ba syn 10.51 y ε 0.517 133Cs
134Ba 2.417% 134Ba is stable with 78 neutrons
135Ba 6.592% 135Ba is stable with 79 neutrons
136Ba 7.854% 136Ba is stable with 80 neutrons
137Ba 11.23% 137Ba is stable with 81 neutrons
138Ba 71.7% 138Ba is stable with 82 neutrons
· r

Barium (play /ˈbɛəriəm/ bair-ee-əm) is a chemical element with the symbol Ba and atomic number 56. It is the fifth element in Group 2, a soft silvery metallic alkaline earth metal. Barium is never found in nature in its pure form due to its reactivity with air. Its oxide is historically known as baryta but it reacts with water and carbon dioxide and is not found as a mineral. The most common naturally occurring minerals are the very insoluble barium sulfate, BaSO4 (barite), and barium carbonate, BaCO3 (witherite). Barium's name originates from Greek barys (βαρύς), meaning "heavy", describing the high density of some common barium-containing ores.

Barium has few industrial applications, but the metal has been historically used to scavenge air in vacuum tubes. Barium compounds impart a green color to flames and have been used in fireworks. Barium sulfate is used for its density, insolubility, and X-ray opacity. It is used as an insoluble heavy additive to oil well drilling mud, and in purer form, as an X-ray radiocontrast agent for imaging the human gastrointestinal tract. Soluble barium compounds are poisonous due to release of the soluble barium ion, and have been used as rodenticides. New uses for barium continue to be sought. It is a component of some "high temperature" YBCO superconductors, and electroceramics.

Contents

Characteristics

Barite

Physical properties

Barium is a soft, silvery white alkali earth metal, which quickly oxidizes in air.[1] It crystallizes in body centered cubic lattices. It burns with a green to pale green flame, resulting from emission at 524.2 and 513.7 nm. Its simple compounds are notable for their relatively high (for an alkaline earth element) specific gravity. This high density is true of the most common barium-bearing mineral, barite (BaSO4), also called 'heavy spar' due to the high density (4.5 g/cm³).

Chemical properties

Barium, as for other alkali earth (group II) metals, is highly reducing. It reacts exothermically with oxygen at room temperature to form barium oxide and peroxide. Because of its sensitivity to air, samples are generally stored under protective oils. The reaction is violent if barium is powdered. The metal is readily attacked in most acids, with the notable exception of sulfuric acid, as passivation stops the reaction by forming the insoluble barium sulfate. It also reacts violently with water according to the reaction:

Ba + 2 H2O → Ba(OH)2 + H2

Barium combines with several metals, including aluminium, zinc, lead and tin, forming intermetallic phases and alloys.[2]

Isotopes

Naturally occurring barium is a mix of seven stable isotopes, the most abundant being 138Ba (71.7 %). 22 isotopes are known, but most of these are highly radioactive and have half-lives in the several millisecond to several day range. The only notable exceptions are 133Ba which has a half-life of 10.51 years, and 137mBa (2.55 minutes).[3] 133Ba is a standard calibrant for gamma-ray detectors in nuclear physics studies.

Occurrence

The abundance of barium is 0.0425 % in the Earth's crust and 13 µg/L in sea water. It occurs in the minerals barite (as the sulfate) and witherite (as the carbonate).[2] Although witherite deposits were mined from the 17th century till 1969[4] in northern England, for example in the Settlingstones Mine near Newbrough,[5] today nearly all barium is mined as barite.

Large deposits of barite are found in China, Germany, India, Morocco, and in the United States.[6] A rare gem containing barium is known, called benitoite.

Production

Trend in world production of barite

Because barium quickly oxidizes in air, it is difficult to obtain the free metal and it is never found free in nature. The metal is primarily found in, and extracted from, barite. Because barite is so insoluble, it cannot be used directly for the preparation of other barium compounds, or barium metal. Instead, the ore is heated with carbon to reduce it to barium sulfide:[7]

BaSO4 + 2 C → BaS + 2 CO2

The barium sulfide is then hydrolyzed or treated with acids to form other barium compounds, such as the chloride, nitrate, and carbonate.

Barium is commercially produced through the electrolysis of molten barium chloride (BaCl2):

(cathode) Ba2+ + 2 e
→ Ba
(anode) 2 Cl → Cl2 + 2 e

Barium metal is also obtained by the reduction of barium oxide with finely divided aluminium at temperatures between 1100 and 1200 °C:

4 BaO + 2 Al → BaO·Al2O3 + 3 Ba

The barium vapor is cooled and condensed to give the solid metal, which can be cast into rods or extruded into wires. Being a flammable solid, it is packaged under argon in steel containers or plastic bags.[2]

Compounds

Ba2+ is the dominant oxidation state throughout the chemistry of barium. Its properties generally resemble those of other alkaline earth ions such as strontium and calcium. All halides, pseudohalides and chalcogenides are known, usually as colourless solids. The sulfate is famously insoluble. BaO forms a peroxide when heated in air. The oxide is basic and reacts with acids to give salts. Barium reduces oxides, chlorides and sulfides of less active metals. For example:

Ba + CdO → BaO + Cd
Ba + ZnCl2 → BaCl2 + Zn
3 Ba + Al2S3 → 3 BaS + 2 Al

At elevated temperatures, barium combines with nitrogen and hydrogen to produce the nitride Ba3N2 and hydride BaH2, respectively. When heated with nitrogen and carbon, it forms the cyanide:

Ba + N2 + 2 C → Ba(CN)2

History

Barium's name originates from Greek βαρύς barys, meaning "heavy", describing the density of some common barium-containing ores. Alchemists in the early Middle Ages knew about some barium minerals. Smooth pebble-like stones of mineral barite found in Bologna, Italy were known as "Bologna stones". Witches and alchemists were attracted to them because after exposure to light they would glow for years.[8]

Carl Scheele identified barite as containing 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 which 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.[9] Davy, by analogy with calcium named "barium" after baryta, with the "-ium" ending signifying a metallic element.[8] Robert Bunsen and Augustus Matthiessen yielded pure barium by electrolysis of a molten mixture of barium chloride and ammonium chloride.[10][11]

The production of pure oxygen in the Brin process was a large scale application of barium peroxide before electrolysis and fractionally distill liquefied air became the dominant ways to produce oxygen. In this process the barium oxide reacts at 500–600°C with air to form barium peroxide which decomposes at above 700°C by releasing oxygen.[12][13]

2 BaO + O2 ⇌ 2 BaO2

Applications

Amoebiasis as seen in radiograph of barium-filled colon
Green barium fireworks

The dominating application of elemental barium is as a scavenger or "getter" removing the last traces of oxygen and other gases in electronic vacuum tubes such as television cathode ray tubes.[2]

An alloy of barium with nickel is commonly used in automobile ignitions.[14]

Applications of barium sulfate

Barium sulfate (the mineral barite, BaSO4) is important to the petroleum industry, for example, as a drilling mud weighting agent in drilling new oil and gas wells.[6] It is also a filler in a variety of products such as rubber. Taking advantage of its opacity to X-rays, the sulfate is used as a radiocontrast agent for X-ray imaging of the digestive system ("barium meals" and "barium enemas").[6] Lithopone, a pigment that contains barium sulfate and zinc sulfide, is a permanent white that has good covering power, and does not darken when exposed to sulfides.[15]

Applications of other barium compounds

Aside from the sulfate, other compounds of barium find only niche applications. Applications are limited by the toxicity of Ba2+ ions (Barium carbonate is a rat poison), which is not a problem for the insoluble BaSO4.

Precautions

Soluble barium compounds are poisonous. At low doses, barium acts as a muscle stimulant, whereas higher doses affect the nervous system, causing cardiac irregularities, tremors, weakness, anxiety, dyspnea and paralysis. This may be due to its ability to block potassium ion channels which are critical to the proper function of the nervous system.[19] However, individual responses to barium salts vary widely, with some being able to handle barium nitrate casually without problems, and others becoming ill from working with it in small quantities. For example, barium acetate was used by Marie Robards to poison her father in 1993.[20]

Non-toxicity of barium sulfate

Because it is highly insoluble in water as well as stomach acids, barium sulfate can be taken orally. It is eliminated completely from the digestive tract. Unlike other heavy metals, barium does not bioaccumulate.[21][22] However, inhaled dust containing barium compounds can accumulate in the lungs, causing a benign condition called baritosis.[23]

See also

References

  1. ^ Stwertka, Albert (2002). A guide to the elements. Oxford University Press US. pp. 144. ISBN 0195150279. 
  2. ^ a b c d Robert Kresse, Ulrich Baudis, Paul Jäger, H. Hermann Riechers, Heinz Wagner, Jochen Winkler, Hans Uwe Wolf, "Barium and Barium Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2007 Wiley-VCH, Weinheim. doi:10.1002/14356007.a03_325.pub2
  3. ^ David R. Lide, Norman E. Holden (2005). "Section 11, Table of the Isotopes". CRC Handbook of Chemistry and Physics, 85th Edition. Boca Raton, Florida: CRC Press. 
  4. ^ Industrial minerals. 1969. p. 28. http://books.google.com/?id=JjEmAQAAIAAJ&dq=Settlingstones+Witherite+Mine&q=Settlingstones+#search_anchor. 
  5. ^ "Alston Moor Cumbria, UK". Steetley Minerals. http://www.rock-site.co.uk/EZ/rs/rs/page151.php. 
  6. ^ a b c d C. R. Hammond (2000). The Elements, in Handbook of Chemistry and Physics 81st edition. CRC press. ISBN 0849304814. 
  7. ^ "Toxicological Profile for Barium and Barium Compounds. Agency for Toxic Substances and Disease Registry". CDC. 2007.. http://www.atsdr.cdc.gov/toxprofiles/tp24.pdf. 
  8. ^ a b Robert E. Krebs (2006). The history and use of our earth's chemical elements: a reference guide. Greenwood Publishing Group. p. 80. ISBN 0313334382. http://books.google.com/?id=yb9xTj72vNAC. 
  9. ^ 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, vol. 98, pages 333-370.
  10. ^ "Masthead". Annalen der Chemie und Pharmacie 93 (3): fmi–fmi. 1855. doi:10.1002/jlac.18550930301. 
  11. ^ 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. 
  12. ^ 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. 
  13. ^ Ihde, Aaron John (1984-04-01). The development of modern chemistry. p. 681. ISBN 9780486642352. http://books.google.de/books?id=34KwmkU4LG0C&pg=PA681. 
  14. ^ Stellman, Jeanne (1998). Encyclopaedia of Occupational Health and Safety: Chemical, industries and occupations. International Labour Organization. pp. 63.8. ISBN 9789221098164. 
  15. ^ Chris J. Jones, John Thornback (2007). Medicinal applications of coordination chemistry. Royal Society of Chemistry. p. 102. ISBN 0854045961. http://books.google.com/?id=uEJHsZWyO-EC. 
  16. ^ Michael S. Russell, Kurt Svrcula (2008). Chemistry of Fireworks. Royal Society of Chemistry. p. 110. ISBN 0854041273. http://books.google.com/?id=yxRyOf8jFeQC. 
  17. ^ 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. 
  18. ^ "Crystran Ltd. Optical Component Materials". http://www.crystran.co.uk/barium-fluoride-baf2.htm. Retrieved 2010-12-29. 
  19. ^ Patnaik, Pradyot (2003). Handbook of inorganic chemicals. pp. 77–78. ISBN 0070494398. http://books.google.com/?id=Xqj-TTzkvTEC&pg=PA243. --
  20. ^ "Boyfriend fight preceded Roanoke mom's slaying". http://www.buffalo.edu/news/pdf/October08/DallanMorningNewsEwingSlaying.pdf. Retrieved 2009-06-06. 
  21. ^ "Toxicity Profiles, Ecological Risk Assessment". US EPA. http://www.epa.gov/region5/superfund/ecology/html/toxprofiles.htm#ba. Retrieved 2009-06-06. 
  22. ^ Moore, J. W. (1991). Inorganic Contaminants of Surface Waters, Research and Monitoring Priorities. New York: Springer-Verlag. 
  23. ^ Doig AT (February 1976). "Baritosis: a benign pneumoconiosis". Thorax 31 (1): 30–9. doi:10.1136/thx.31.1.30. PMC 470358. PMID 1257935. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=470358. 

External links


Translations:

Barium

Top

Dansk (Danish)
n. - barium

Nederlands (Dutch)
barium(sulfaat)

Français (French)
n. - baryum, (Méd) sulfate de baryum

Deutsch (German)
n. - (chem.) Barium

Ελληνική (Greek)
n. - βάριο

Italiano (Italian)
bario

Português (Portuguese)
n. - bário (m) (Quím.)

Русский (Russian)
барий

Español (Spanish)
n. - bario

Svenska (Swedish)
n. - barium

中文(简体)(Chinese (Simplified))

中文(繁體)(Chinese (Traditional))
n. - 鋇

한국어 (Korean)
n. - 바륨(금속원소의 하나)

日本語 (Japanese)
n. - バリウム

العربيه (Arabic)
‏(الاسم) مادة الباريوم‏

עברית (Hebrew)
n. - ‮בריום (מתכת)‬


 
 

 

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