Tetraethyl lead

From Citizendium, the Citizens' Compendium
Jump to: navigation, search
This article is developing and not approved.
Main Article
Talk
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and not meant to be cited; by editing it you can help to improve it towards a future approved, citable version. These unapproved articles are subject to a disclaimer.
Properties
Property Value
Common name tetraethyl lead
Other names tetra-ethyl lead, lead tetraethyl, TEL
IUPAC name tetraethylplumbane
CAS number 78-00-2
Molecular formula (CH3CH2)4Pb
Molecular mass 323.4 g/mol[1]
Density 1.653 g/ml for liquid at 20 °C, 1 atm[2]
Boiling point 455.7 K (182.6 °C) at 1 atm[1]
Melting point 142.94 K (-130.2 °C)[1]
Flash point 366.48 K (93.3 °C)[2]
Specific heat, cp 0.956 J/(g·K) for liquid at 20 °C[1]
Heat of vaporization 175.0 J/g for liquid at 182.6 °C[1]
Heat of fusion 27.2 J/g for solid at -130.2 °C[1]
Viscosity 0.862 mPa·s (0.862 cP) at 20 °C[3]
Refractive index 1.5198 nD20 [4]

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[5] 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.

TEL is still available for use as an additive to increase the octane rating of aviation fuel for aircraft powered by internal combustion engines.

Manufacture and properties

Pure tetraethyl lead, as distinguished from tetraethyl lead fluid (TEL fluid), is a viscous, colorless liquid that is highly lipophilic and soluble in fats, oils and lipids as well as gasoline and other non-polar hydrocarbons.

The various other physical and chemical properties of tetraethyl lead are listed in the adjacent table.

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

At the temperatures found in spark-ignited internal combustion engines, TEL decomposes completely into lead and lead oxide (PbO) and combustible, short-lived ethyl radicals. Lead itself is the reactive agent that enhances the octane rating of gasolines and tetraethyl lead serves as a gasoline-soluble lead carrier.

TEL fluid formulation

When TEL burns, it produces not only carbon dioxide (CO2) and water (H2O), but also lead (Pb):

(CH3CH2)4Pb + 13 O2 → 8 CO2 + 10 H2O + Pb

The lead can the oxidize further to give lead oxide (PbO):

2 Pb + O2 → 2 PbO

The Pb and PbO would soon accumulate and destroy an engine. For this reason, the TEL used in gasoline was actually part of a blended liquid formulation known as TEL fluid or ethyl fluid that contained 1,2-dibromoethane and 1,2-dichloroethane liquids known as lead scavengers. Those scavengers formed lead bromide (PbBr) and lead chloride (PbCl) which are volatile and were emitted from the engine exhaust to the atmosphere. The complete composition of TEL fluid was:[6]

  • Tetraethyl lead       61.45%
  • 1,2-Dibromoethane 17.85%
  • 1,2-Dichloroethane 18.80%
  • Inerts & color dye    1.90%

The addition of as little as 0.8 ml of TEL fluid per liter of gasoline (3 ml/gallon) of gasoline was equivalent to adding 0.5 g of lead per liter of gasoline and resulted in significant increases in the octane rating of the gasoline.

History of tetraethyl lead as a gasoline octane enhancer

For more information, see: Lead, Gasoline, and Octane rating.
(CC) Photo: Dan Plazak
Sign on an ancient gasoline pump advertising tetraethyllead by the Ethyl Corporation.

In the 1920's, petroleum refining technology was rather primitive and produced gasolines with an octane rating of about 40 – 60. But automotive engines were rapidly being improved and required better gasolines, which led to a search for octane rating enhancers. That search culminated in 1921[7][8][9]n the development and use of tetraethyl lead as an octane enhancer.

Its utility was discovered by Kettering and Thomas Midgely Jr. By 1923, "When Thomas Midgley accepted the Nichols Medal in March, 1923, he had almost returned to normal after fighting a winter-long battle with lead poisoning." Cite error: Invalid <ref> tag; invalid names, e.g. too many Despite ethanol being widely recognized as an alternative octane rating enhancer, [10] the less expensive TEL quickly became commercially available as what was called TEL fluid, which contained 61.5 weight % TEL. The addition of as little as 0.8 ml of that TEL fluid per litre (equivalent to 0.5 gram of lead per litre) of gasoline resulted in significant octane rating increases.

In 1924, New York City Medical Examiner Charles Norris, and his forensic chemist, Alexander Gettler, were asked to investigate possible occupational exposure and toxicity in a plant in New Jersey, recently opened by Standard Oil. Workers called the TEL facility the "looney gas building" because hallucinations were common. Within a year, 32 of 49 TEL workers were hospitalized and 5 were dead. The building manager said "these men probably went insane becayse they were working too hard." Thomas Midgely Jr., the General Motors engineer that worked out the needed TEL concentration, put his hand in a bowl of TEL, saying "I'm taking no chances whatsoever. Nor would I take any chances doing that every day." Midgely, a few months after the press conference, traveled to Europe for treatment of lead poisoning.[11]

Production and sale of "leaded gas" was briefly banned in 1925 by the Surgeon General,[10] and a panel of experts was appointed to investigate a number of fatalities that had "occurred in the manufacture and mixing of the concentrated tetraethyl lead". In 1927, the Surgeon General set a voluntary standard for the petroleum refining industry to follow in mixing tetraethyl lead with gasoline. The standard was 3 cubic centimeters per gallon (cm3/gal), corresponding to the maximum then in use among refiners, and thus imposed no real restraint. [9]

For about the next 50 years, TEL was used as the most cost effective way to raise the octane rating of gasolines. During that period, petroleum refining technology grew until high-octane gasolines could, in fact, be produced without using TEL. Also, in about the 1940's, it was discovered that the lead being emitted in the exhaust gases from vehicular internal combustion engines was a toxic air pollutant that seriously affected human health.

Because of its toxicity and the fact that catalytic converters being installed in vehicles could not tolerate the presence of lead, the U.S. EPA launched an initiative in 1972 to phase out the use of TEL in the United States and it was completely banned for use in on-road vehicles as of January 1996.[12] [13] Using TEL in race cars, airplanes, marine engines and farm equipment is still permitted. TEL usage has also been phased out by most nations worldwide. As of 2008, the only nations still allowing extensive use of TEL are the Democratic People's Republic of Korea, Burma, and Yemen.[14][15]

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 NIST Chemistry WebBook
  2. 2.0 2.1 Tetraethyl lead, liquid] From the website of the National Oceanic and Atmospheric Administration (NOAA)
  3. Tetraethyl lead From the website of the National Oceanic and Atmospheric Administration (NOAA)
  4. Béla G. Lipták (2003). Instrument Engineers' Handbook, 4th Edition. CRC Press. 0-8493-1083-0. 
  5. Phasing Lead Out of Gasoline A report issued by the United Nations Environmental Programme (UNEP). See page 8 of 23 pdf pages.
  6. Historical Uses A publication of the U.S. Environmental Protection Agency
  7. The Rise and Fall of Tetraethyllead Dietmar Seyferth, Department of Chemistry, Massachusetts Institute of Technology, Organometallics, 2003, 22 (25), pp 5154–5178
  8. Definition of Tetraethyl Lead
  9. 9.0 9.1 Lead Poisoning: A Historical Perspective
  10. 10.0 10.1 Ethyl-leaded gasoline
  11. Deborah Blum (18 February 2010), The Poisoner's Handbook: Murder and the Birth of Forensic Medicine in Jazz Age New York, Penguin Press, ISBN 978-1594202438, pp. 120-124
  12. Phasing Lead Out of Gasoline a report issued by the United Nations Environmental Programme (UNEP)
  13. Prohibition on Gasoline Containing Lead or Lead Additives for Highway Use From the website of the U.S. Environmental Protection Agency
  14. Asia-Pacific Lead Matrix a report issued by the United Nations Environmental Programme (UNEP)
  15. West Asia, Middle East and North Africa Lead Matrix a report issued by the United Nations Environmental Programme (UNEP)