James
J. Spivey
Research
Our research focuses on the development and characterization of
heterogeneous catalysts. Because these catalysts are used in the
production of virtually all organic chemicals and fuels, as well
as in many environmental applications, the study of these materials
is an essential element in meeting the challenges facing chemical
engineers.
One part of our research focuses on environmental catalysis. An
example is the development of catalysts as part of a fuel processing
system that will allow current fuels such as gasoline and diesel
to be used to produce hydrogen for automobiles powered by fuel cells.
These types of automobiles produce extremely low emissions and are
more efficient than those based on combustion engines. There are
significant catalyst and reactor design challenges that must be
met, however. Catalysts must be active, selective for the specific
reaction of interest, and deactivate at very low rates. We synthesize,
test, and develop kinetic models for supported metal catalysts for
reactions such as the selective oxidation of carbon monoxide, which
purifies the hydrogen stream immediately upstream of the fuel cell.
The demands of an automobile -compact reactor size, response to
transient demands, and severe thermal cycles- also require innovative
reactor design. We are working to find new ways of designing catalytic
reactors to meet these demands.
Another example of environmental catalysis is the catalytic decomposition
of nitric oxide, NO, which is present in engine exhausts and is
an atmospheric pollutant. Although the decomposition of NO to nitrogen
and oxygen is thermodynamically favored at the conditions present
in exhaust gases, no practical catalyst has yet been developed that
can carry out this reaction. Most catalysts are either poisoned
by oxygen or deactivate rapidly in the presence of water vapor,
which is also present in exhaust gases. We are carrying out research
to understand the fundamental processes on the catalyst surface
to help us develop a catalyst for this reaction. A second approach
NO control is to catalytically oxidize NO to NO2, react this with
a solid base to form a nitrate, and periodically pulse the nitrate
with a reducing gas produced from the fuel. Though this is more
complex than decomposing NO, this is one way to remove NO from exhaust
gases. We are also studying materials for this process.
A second area of our research focuses on synthesis of chemical
intermediates from simple carbon feedstocks such as methane. An
example is the direct, stoichiometric synthesis of acetic acid from
methane and CO2. This reaction has recently been demonstrated by
one of our students. The low equilibrium yield of the reaction at
all practical conditions, however, requires innovative approaches
that will overcome this limitation, by reacting the acetic acid
to further products, for example. The catalysts and reaction conditions
for this synthesis reaction are being studied.
A final example that combines both types of catalysis is the synthesis
of ultra-clean fuels using the Fischer Tropsch process. This process
converts synthesis gas (a mixture of hydrogen and CO, derived from
a number or feedstocks such as natural gas or coal) into liquid
fuels. Although this process was originally developed a number of
years ago, there are still significant research needs-including
catalysts and reactor designs that maximize the yield of the desirable
fuels and minimize the yield of low-value byproducts.
My research interests also include the application of the principles
of heterogeneous catalysis to catalytic combustion, control of sulfur
and nitrogen oxides from combustion processes, acid/base catalysis
(e.g., for condensation reactions), hydrocarbon synthesis, and the
study of catalyst deactivation.
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This page was last modified on September 2, 2002
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