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Contents

   



(Top)
 


1Preparation
 




2Reactions
 




3Uses
 


3.1Other uses
 






4References
 




5External links
 













Barium carbonate






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Barium carbonate
Skeletal formula of barium carbonate
Powder of barium carbonate
Names
Other names

Witherite

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • ChEBI
    ChemSpider
    ECHA InfoCard 100.007.426 Edit this at Wikidata
    EC Number
    • 208-167-3

    PubChem CID

    RTECS number
    • CQ8600000
    UNII
    UN number 1564

    CompTox Dashboard (EPA)

    • InChI=1S/CH2O3.Ba/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2 checkY

      Key: AYJRCSIUFZENHW-UHFFFAOYSA-L checkY

    • InChI=1/CH2O3.Ba/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2

      Key: AYJRCSIUFZENHW-NUQVWONBAT

    • [Ba+2].[O-]C([O-])=O

    • C(=O)([O-])[O-].[Ba+2]

    Properties

    Chemical formula

    BaCO3
    Molar mass 197.34 g/mol
    Appearance white crystals
    Odor odorless
    Density 4.286 g/cm3
    Melting point 811 °C (1,492 °F; 1,084 K)
    polymorphic transformation
    Boiling point 1,450 °C (2,640 °F; 1,720 K)
    decomposes[1] from 1360 °C

    Solubility in water

    16 mg/L (8.8°C)
    22 mg/L (18 °C)
    24 mg/L (20 °C)
    24 mg/L (24.2 °C)[1]

    Solubility product (Ksp)

    2.58·10−9
    Solubility decomposes in acid
    insoluble in methanol

    Magnetic susceptibility (χ)

    -58.9·10−6cm3/mol

    Refractive index (nD)

    1.676
    Structure

    Crystal structure

    orthorhombic
    Thermochemistry

    Heat capacity (C)

    85.35 J/mol·K[1]

    Std molar
    entropy
    (S298)

    112 J/mol·K[2]

    Std enthalpy of
    formation
    fH298)

    -1219 kJ/mol[2]

    Gibbs free energy fG)

    -1139 kJ/mol[1]
    Hazards
    GHS labelling:

    Pictograms

    GHS07: Exclamation mark[3]

    Signal word

    Warning

    Hazard statements

    H302[3]
    NFPA 704 (fire diamond)
    NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
    2
    0
    0
    Flash point Non-flammable
    Lethal dose or concentration (LD, LC):

    LD50 (median dose)

    418 mg/kg, oral (rat)
    Safety data sheet (SDS) ICSC 0777
    Related compounds

    Other cations

    Beryllium carbonate
    Magnesium carbonate
    Calcium carbonate
    Strontium carbonate
    Radium carbonate

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Barium carbonate is the inorganic compound with the formula BaCO3. Like most alkaline earth metal carbonates, it is a white salt that is poorly soluble in water. It occurs as the mineral known as witherite. In a commercial sense, it is one of the most important barium compounds.[5]

    Preparation[edit]

    Barium carbonate is made commercially from barium sulfide by treatment with sodium carbonate at 60 to 70 °C (soda ash method) or, more commonly carbon dioxide at 40 to 90 °C:

    In the soda ash process, an aqueous solution of barium sulfide is treated with sodium carbonate:[5]

    BaS + H2O + CO2 → BaCO3 + H2S

    Reactions[edit]

    Barium carbonate reacts with acids such as hydrochloric acid to form soluble barium salts, such as barium chloride:

    BaCO3 + 2 HCl → BaCl2 + CO2 + H2O

    Pyrolysis of barium carbonate gives barium oxide.[6]

    Uses[edit]

    It is mainly used to remove sulfate impurities from feedstock of the chlor-alkali process. Otherwise it is a common precursor to barium-containing compounds such as ferrites.[5]

    Other uses[edit]

    Barium carbonate is widely used in the ceramics industry as an ingredient in glazes. It acts as a flux, a matting and crystallizing agent and combines with certain colouring oxides to produce unique colours not easily attainable by other means. Its use is somewhat controversial since it can leach from glazes into food and drink. To reduce toxicity concerns, it is often substituted with strontium carbonate, which behaves in a similar way in glazes but is of lower toxicity.

    In the brick, tile, earthenware and pottery industries barium carbonate is added to clays to precipitate soluble salts (calcium sulfate and magnesium sulfate) that cause efflorescence.

    It is sometimes used as an "energiser" in the Case-hardening process.

    References[edit]

    1. ^ a b c d "Barium carbonate". Archived from the original on 2014-05-06. Retrieved 2014-05-06.
  • ^ a b Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. ISBN 978-0-618-94690-7.
  • ^ a b Sigma-Aldrich Co., Barium carbonate. Retrieved on 2014-05-06.
  • ^ Sciences labs MSDS
  • ^ a b c Kresse, Robert; Baudis, Ulrich; Jäger, Paul; Riechers, H. Hermann; Wagner, Heinz; Winkler, Jochen; Wolf, Hans Uwe (2007). "Barium and Barium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_325.pub2. ISBN 978-3527306732.
  • ^ P. Ehrlich (1963). "Barium Oxide". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 1. NY, NY: Academic Press. pp. 933–944.
  • External links[edit]

    "Preparation and Characterization of Barium Carbonate Nanoparticles - Volume 2 Number 4 (Aug. 2011) - IJCEA". www.ijcea.org. Retrieved 2017-12-13.


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Barium_carbonate&oldid=1225855806"

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