Lithium carbide

Lithium carbide
Lithium carbide
Identifiers
CAS number 1070-75-3
ChemSpider 59503 YesY
EC number 213-980-1
Jmol-3D images Image 1
Properties
Molecular formula Li2C2
Molar mass 37.9034 g/mol
Density 1.3 g/cm³[1]
Melting point

> 550°C

 YesY carbide (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Lithium carbide, Li2C2, often known as dilithium acetylide, is a chemical compound of lithium and carbon, an acetylide. It is an intermediate compound produced during radiocarbon dating procedures. Li2C2 is one of an extensive range of lithium-carbon compounds which include the lithium-rich Li4C, Li6C2, Li8C3, Li6C3, Li4C3, Li4C5, and the graphite intercalation compounds LiC6, LiC12, and LiC18.
Li2C2 is the thermodynamically-stable lithium-rich compound and is the only one of them that can be obtained directly from the elements. It was first produced by Moissan, in 1896[2] who reacted coal with lithium carbonate. The other lithium-rich compounds are produced by reacting lithium vapor with chlorinated hydrocarbons, e.g. CCl4.

Lithium carbide is sometimes confused with the drug lithium carbonate, Li2CO3, because of the similarity of its name.

Contents

Structure

Li2C2 is a salt formulated 2Li+C22−. It has a similar structure to that of edit] Preparation and chemistry

To prepare pure samples in the laboratory molten lithium + graphite are reacted at high temperature. Li2C2 can also be prepared by reacting CO2 with molten lithium. It is reactive and hydrolyses very readily to form acetylene gas, C2H2, and LiOH.

Use in radiocarbon dating

There are a number of procedures employed, some that burn the sample producing CO2 that is then reacted with lithium, and others where the carbon containing sample is reacted directly with lithium metal.[4] The outcome is the same: Li2C2 is produced, which can then be used to create species easy to mass, like acetylene and benzene.[5] Note that lithium nitride may be formed and this produces ammonia when hydrolyzed, which contaminates the acetylene gas.

References

  1. ^ R. Juza; V. Wehle; H.-U. Schuster (1967). "Zur Kenntnis des Lithiumacetylids". Zeitschrift für anorganische und allgemeine Chemie 352: 252. doi:10.1002/zaac.19673520506. 
  2. ^ H. Moissan Comptes Rendus hebd. Seances Acad. Sci. 122, 362 (1896)
  3. ^ U. Ruschewitz, R. Pöttgen (1999). "Structural Phase Transition in Li2C2". Zeitschrift für anorganische und allgemeine Chemie 625 (10): 1599–1603. doi:10.1002/(SICI)1521-3749(199910)625:10<1599::AID-ZAAC1599>3.0.CO;2-J. 
  4. ^ Swart E.R. (1964). "The direct conversion of wood charcoal to lithium carbide in the production of acetylene for radiocarbon dating". Cellular and Molecular Life Sciences 20: 47. doi:10.1007/BF02146038. 
  5. ^ University of Zurich Radiocarbon Laboratory webpage

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