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Volumn 22, Issue 25, 2003, Pages 5154-5178

The Rise and Fall of Tetraethyllead. 2

Author keywords

[No Author keywords available]

Indexed keywords

ANTIKNOCK AGENTS; AVIATION FUELS; KNOCK INHIBITORS;

EID: 0348040035     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om030621b     Document Type: Review
Times cited : (73)

References (156)
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    • (b) Robert, J. C. Ethyl. A History of the Corporation and the People Who Made It; University Press of Virginia; Charlottesville, VA, 1983 (the tetraethyllead story from the point of view of industry)
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    • (j) Kitman, J. L., The Secret History of Lead, The Nation 2000, March 20 issue (http/www.thenation.com/doc.mhtml?i=20000320&s=kitman) (a lengthy review with a strong anti-industry bias)
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    • A correction is needed: C. J. Löwig was a professor at the University of Zürich, which was founded in 1833 (not the ETH in Zürich, which was founded in 1854). My thanks to Prof. Albrecht Salzer for pointing this out
    • Seyferth, D. Organometallics 2003, 22, 2346. A correction is needed: C. J. Löwig was a professor at the University of Zürich, which was founded in 1833 (not the ETH in Zürich, which was founded in 1854). My thanks to Prof. Albrecht Salzer for pointing this out.
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    • first scientific publication on the antiknock effect of tetraethyllead
    • (a) Midgley, T., Jr.; Boyd, T. A. Ind. Eng. Chem. 1922, 14, 897 (first scientific publication on the antiknock effect of tetraethyllead).
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    • Midgley Jr., T.1    Boyd, T.A.2
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    • U.S. Patent 1,573,846 (Feb. 23, 1926) (Figure 7), application Apr. 15, 1922, was awarded to Midgley. A Midgley patent, U.S. 1,592,954 (July 20, 1926), disclosing the use of an organohalogen scavenger in leaded gasoline followed soon after
    • (b) U.S. Patent 1,573,846 (Feb. 23, 1926) (Figure 7), application Apr. 15, 1922, was awarded to Midgley. A Midgley patent, U.S. 1,592,954 (July 20, 1926), disclosing the use of an organohalogen scavenger in leaded gasoline followed soon after.
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    • This was written when Calingaert, a Belgian, was a member of the Research Laboratory of Applied Chemistry at M.I.T. He later joined Ethyl Gasoline Corp., ultimately becoming Director of Chemical Research
    • (a) Calingaert, G. Chem. Rev. 1925, 2, 43. This was written when Calingaert, a Belgian, was a member of the Research Laboratory of Applied Chemistry at M.I.T. He later joined Ethyl Gasoline Corp., ultimately becoming Director of Chemical Research
    • (1925) Chem. Rev. , vol.2 , pp. 43
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    • U.S. Patent 1,622,228 (March 22, 1927)
    • (b) See also: Midgley, T., Jr. U.S. Patent 1,622,228 (March 22, 1927).
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    • Niohols Award address
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    • Scientific Memoirs series; National Academy of Sciences, National Academy Press: Washington, DC
    • (a) Fuoss, R. A. Biographical Memoirs; Scientific Memoirs series; National Academy of Sciences, National Academy Press: Washington, DC, 1971; Vol. 42, p 119.
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    • Reference 1c
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    • U.S. Patents 1,612,131 (Dec 28, 1926), 1,690,075 (Oct 30, 1928), 1,697,245 (Jan 1, 1929), and 1,694,268 (Dec 4, 1928)
    • Kraus, C. A.; Callis, C. C. U.S. Patents 1,612,131 (Dec 28, 1926), 1,690,075 (Oct 30, 1928), 1,697,245 (Jan 1, 1929), and 1,694,268 (Dec 4, 1928).
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    • Public Health Bulletin No. 163; U.S. Public Health Service, Treasury Department: Washington, DC
    • (a) The Use of Tetraethyl Lead Gasoline in its Relation to Public Health; Public Health Bulletin No. 163; U.S. Public Health Service, Treasury Department: Washington, DC, 1926.
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    • (b) For an account of the first industrial experiences with tetraethyllead toxicity and the reactions of industry, the government, and public health advocates, see: Needleman, H. L. Environ. Res. 1997, 74, 95.
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    • Needleman, H.L.1
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    • References le-g
    • 5Cl/NaPb reaction see: (a) References le-g.
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    • Advances in Chemistry Series 23; American Chemical Society: Washington, DC
    • (b) Shapiro, H. In Metal-Organic Compounds; Advances in Chemistry Series 23; American Chemical Society: Washington, DC, 1959; pp 290-298.
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    • Shapiro, H.1
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    • Chemical Process Monograph No. 20; Noyes Development Corp.: Park Ridge, NJ, details gleaned from the patent literature. The discussion in the text which follows is based mostly on the information provided by Shapiro and Frey in refs le and 19b
    • (d) Sittig, M. Organometallics; Chemical Process Monograph No. 20; Noyes Development Corp.: Park Ridge, NJ, 1966; pp 67-104 (details gleaned from the patent literature). The discussion in the text which follows is based mostly on the information provided by Shapiro and Frey in refs le and 19b.
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    • Petz, W., Vol. Ed.; Gmelin Institut für Anorganische Chemie der Max-Planck-Gesellschaft zur Förderung der Wissenschaften and Springer-Verlag: Berlin, xii + 194 pages. Unfortunately, a similar volume devoted to tetraethyllead will not be published, since the Gmelin Institute has been discontinued
    • All the reader might want to know about tetramethyllead, with an abundance of references, is given in: Huber, P. Gmelin Handbook of Inorganic Chemistry, 8th ed.; Pb. Organolead Compounds. Part 1. Tetramethyllead; Petz, W., Vol. Ed.; Gmelin Institut für Anorganische Chemie der Max-Planck-Gesellschaft zur Förderung der Wissenschaften and Springer-Verlag: Berlin, 1987; xii + 194 pages. Unfortunately, a similar volume devoted to tetraethyllead will not be published, since the Gmelin Institute has been discontinued.
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    • (b) Details are given in: Blitzer, S. M.; Pearson, T. H. U.S. Patents 2,859,225-2,859,232 (Nov 4,1958)
    • Blitzer, S.M.1    Pearson, T.H.2
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    • U.S. Patent 2,-818,417 (Dec 31, 1957) (application July 11, 1955)
    • (a) Brown, J. E.; Shapiro, H.; De Witt, E. G., U.S. Patent 2,-818,417 (Dec 31, 1957) (application July 11, 1955).
    • Brown, J.E.1    Shapiro, H.2    De Witt, E.G.3
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    • Reinhold: New York
    • (g) In the early 1960s Ethyl's TEL Motor 33 Mix for blending with gasoline contained about 57.5% tetraethyllead, 7.0% methylcyclopentadienylmanganese tricarbonyl, 17.6% 1,2-dichloroethane, 16.7% 1,2-dibromoethane, and 1.2% dye: Harwood, J. H. Industrial Applications of the Organometallic Compounds; Reinhold: New York, 1963; p 127.
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    • Examples from the patent literature are given in refs If and 35.
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    • This is just one of many such studies carried out around this time
    • Otto, K.; Montreuil, C. N. Environ. Sci. Technol. 1976, 10, 154. This is just one of many such studies carried out around this time.
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    • Advances in Chemistry Series 23; American Chemical Society: Washington, DC, See also refs 1e,f
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    • Apropos these data, it is of interest to read what the Octel website (http://www.octel-corp.oom/products/leadalkyls/leadalkyls.htm) says: "As the world's leading producer of tetraethyl lead (TEL), Octel recognises that reductions in the amount of lead present in the man-made environment, from which few overall benefits result, represent a prudent step forward in terms of environmental management. The transition by refineries to unleaded gasoline due to environmental concerns and its incompatibility with the catalyst in catalytic converters will inevitably take some time. During this period, the economies of some countries will continue to depend on leaded gasoline and TEL. Octel remains committed to maintaining a professional working partnership with these customers to ensure the continuity of its supply during the phase-out period."


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