William
Kovarik |
Fuels and Society: 12. Additives/Tetraethyllead |
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| Back to: 10. Knocking Back to: 11. Alcohol Fuel as a Replacement Ahead to 17. TEL Toxicity Ahead to 13. Kettering and Midgley Back to Concept Map
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12. Additives / TEL Most fuel research within the oil industry involved new ways to create branched chain hydrocarbons in the less volatile fractions of the fuel. Oil industry researchers found that if petroleum was cooked long enough, with enough pressure, and run through the right catalyst, a higher quality anti-knock fuel would result. This trend in research did, in fact, result in the largest increase in anti-knock quality over the years. Charles F. Kettering, on the other hand, was working on research problems for the automotive industry. His Dayton Metal Products Co. was merged with General Motors in 1919 and became the core of GM's research division.
Ketterings fuel research had opened two very interesting doors. The high percentage solutions alcohol and benzene -- appear to be very promising allies to petroleum, Ketterings assistants Thomas Midgley and T.A. Boyd said..[i] Alcohol was the most direct route ... for converting energy from its source, the sun, into a material that is suitable for a fuel... But alcohol from food crops involved supply problems. Only celluosic biomass had the potential to compete with petroleum over the long run, they believed. The second door -- thelow
percentage class of solution -- was originally
represented by iodine. It was far too expensive to be
practical, but it led to experiments in 1920 and 1921
that would change the automotive world. The experiments were guided by a
peg board with a portion of the periodic table of
elements pasted on it. The board helped the researchers
compare their tests of already known knock suppressors
(such as bromine, iodine, tellurium, tin and
selenium) and new fuel additives (such as arsenic and
sulfur). Historians have seen it as a beautiful
piece of pure research. The atmosphere in the labs grew
more expectant as the pegboard seemed to point the
way toward the heavy end of the carbon group: silicon,
germanium, tin and lead. Visiting his father in
Massachusetts in late October, Midgley had
antiknock results from each new test sent via telegraph
daily. Tetraethyl tin proved effective, but even
more exciting was the prospect of metallic lead at
the bottom of the column on the peg board. When the chemists finally
delivered a small amount of tetraethyl lead on the
morning of December 9, 1921, the knock in the
one-cylinder laboratory engine was utterly silenced. Even
diluted to a strength of two or three grams per gallon,
or one thousand to one, tetraethyl lead had a remarkable
ability to quiet the relentless knocking.
Midgley, Boyd and others in the lab danced
a very unscientific jig and hurried off to include
Kettering in their victory party. Holding a test
tube full of the stuff in his fingers, Kettering
suggested, perhaps ironically, the name ethyl
for the chemical compound tetraethyl lead. Although the
term referred to the ethyl alcohol solvent used to
dissolve the lead, and utterly confused the question of
high percentage versus low percentage solutions, the name
Ethyl stuck. [i] Large-scale production of benzene
was questionable. Even if all the coal mined in the U.S.
in 1920 were used to supply benzene, only about 900
million gallons, or one-fifth of the U.S. gasoline supply
would be replaced, he said. |
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