Tetraethyl lead: Difference between revisions
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| align="left"|'''Heat of fusion'''|| align="left"|27.2 J/g for solid at -130.2 °C<ref name=NIST/> | | align="left"|'''Heat of fusion'''|| align="left"|27.2 J/g for solid at -130.2 °C<ref name=NIST/> | ||
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| align="left"|'''Viscosity'''||align="left"| | | align="left"|'''Viscosity'''||align="left"|0.862 mPa·s (0.862 cP) at 20 °C<ref>[http://cameochemicals.noaa.gov/chris/TEL.pdf Tetraethyl lead] From the website of the [[National Oceanic and Atmospheric Administration (NOAA)]]</rerf> | ||
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| align="left"|'''Refractive index'''||align="left"|1.5198 ''n''<sub>D</sub><sup>20</sup> | | align="left"|'''Refractive index'''||align="left"|1.5198 ''n''<sub>D</sub><sup>20</sup> |
Revision as of 22:06, 20 May 2009
Tetraethyl lead (TEL) is a liquid with the chemical formula (CH3CH2)4Pb. Once widely used (circa 1925 to 1990) to increase the octane rating of gasoline (petrol), TEL usage in gasoline has been largely phased out by most nations[1] primarily because of the toxicity of the lead emissions from spark-ignited internal combustion engines burning gasoline containing TEL. Another reason for discontinuing TEL usage was that it degraded the efficiency of the catalytic converters installed in automotive vehicles to reduce their emissions of air pollutants.
Manufacture and properties
TEL is produced by the alkylation of a sodium-lead alloy using chloroethane as expressed by this chemical equation:
- 4 CH3CH2Cl + 4 NaPb → (CH3CH2)4Pb + 4 NaCl + 3 Pb
which can also be written as:
- 4 moles of chloroethane + 4 moles of sodium-lead alloy → 1 mole of tetraethyl lead + 4 moles of sodium chloride + 3 moles of lead
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