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Carbonate

Related subjects: Chemical compounds

Background Information

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Ball-and-stick model of the carbonate ion, CO32−

In chemistry, a carbonate is a salt or ester of carbonic acid.

Applications

Soda water (also known as Seltzer water) is water with CO2 dissolved under pressure. The taste of soda water was discovered by the 18th century chemist Joseph Priestley.

To test for the presence of the carbonate anion in a salt, the addition of dilute mineral acid (e.g. hydrochloric acid) will yield carbon dioxide gas.

Carbonate-containing salts are industrially and mineralogically ubiquitous. The term "carbonate" is also commonly used to refer to one of these salts or carbonate minerals. Most common is calcite, or calcium carbonate, the chief constituent of limestone. The process of removing carbon dioxide from these salts by heating is called calcination.

The term is also used as a verb, to describe the process of raising carbonate and bicarbonate concentrations in water, see also carbonated water, either by the introduction under pressure of carbon dioxide gas into the water, or by dissolving carbonate or bicarbonate salts into the water.

Chemical properties

The carbonate ion is a polyatomic anion with the empirical formula CO32− and a molecular mass of 60.01 daltons; it consists of one central carbon atom surrounded by three identical oxygen atoms in a trigonal planar arrangement. The carbonate ion carries a negative two formal charge and is the conjugate base of the hydrogen carbonate ion, HCO3, which is the conjugate base of H2CO3, carbonic acid.

A carbonate salt forms when a positively charged ion attaches to the negatively charged oxygen atoms of the ion, forming an ionic compound. Most carbonate salts are insoluble in water at standard temperature and pressure, with solubility constants of less than 1×10−8. Exceptions include sodium, potassium and ammonium carbonates.

In aqueous solution, carbonate, bicarbonate, carbon dioxide, and carbonic acid exist together in a dynamic equilibrium. In strongly basic conditions, the carbonate ion predominates, while in weakly basic conditions, the bicarbonate ion is prevalent. In more acid conditions, aqueous carbon dioxide, CO2(aq), is the main form, which, with water, H2O, is in equilibrium with carbonic acid - the equilibrium lies strongly towards carbon dioxide. Thus sodium carbonate is basic, sodium bicarbonate is weakly basic, while carbon dioxide itself is a weak acid.

Carbonated water is formed by dissolving CO2 in water under pressure. When the partial pressure of CO2 is reduced, for example when a can of soda is opened, the equilibrium for each of the forms of carbonate (carbonate, bicarbonate, carbon dioxide, and carbonic acid) shifts until the concentration of CO2 in the solution is equal to the solubility of CO2 at that temperature and pressure. In living systems an enzyme, carbonic anhydrase, speeds the interconversion of CO2 and carbonic acid.

In organic chemistry a carbonate can also refer to a functional group within a larger molecule that contains a carbon atom bound to three oxygen atoms, one which is double bonded. The VSEPR shape of the carbonate ion is trigonal planar or triplanar

Acid-base chemistry

The carbonate ion (CO32−) is a strong base. It is a conjugate base of the weakly acidic bicarbonate ( IUPAC name hydrogen carbonate HCO3), itself a strong conjugate base of the still weakly acidic carbonic acid. As such in aqueous solution, the carbonate ion seeks to reclaim hydrogen atoms.

It works as a buffer in the blood as follows: when pH is too low, the concentration of hydrogen ions is too high, so you exhale CO2. This will cause the equation to shift left, essentially decreasing the concentration of H+ ions, causing a more basic pH.

When pH is too high, the concentration of hydrogen ions in the blood is too low, so the kidneys excrete bicarbonate (HCO3). This causes the equation to shift right, essentially increasing the concentration of hydrogen ions, causing a more acidic pH.

Carbonate salts

  • Carbonate overview:
H2CO3 He
Li2CO3 BeCO3 B C N O F Ne
Na2CO3 MgCO3 Al2(CO3)3 Si P S Cl Ar
K2CO3 CaCO3 Sc Ti V Cr MnCO3 FeCO3 CoCO3 NiCO3 CuCO3 ZnCO3 Ga Ge As Se Br Kr
Rb2CO3 SrCO3 Y Zr Nb Mo Tc Ru Rh Pd Ag2CO3 CdCO3 In Sn Sb Te I Xe
Cs2CO3 BaCO3 Hf Ta W Re Os Ir Pt Au Hg Tl2CO3 PbCO3 Bi Po At Rn
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Cn Uut Fl Uup Lv Uus Uuo
La2(CO3)3 Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr



History

It is generally thought that the presence of carbonates in rock is unequivocal evidence for the presence of liquid water. Recent observations of the Planetary nebula NGC 6302 shows evidence for carbonates in space , where aqueous alteration similar to that on Earth is unlikely. Other minerals have been proposed which would fit the observations.

Significant carbonate deposits have not been found on Mars via remote sensing or in situ missions, even though Martian meteorites contain small amounts and groundwater may have existed at both Gusev and Meridiani Planum.

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